SEQUENCE LISTING SUBMISSION ON COMPACT DISC [0002] The Sequence Listing submitted concurrently herewith on compact disc under 37 C. F. R. §§1. 821 (c) and 1.821 (e) is herein incorporated by reference in its entirety. Three copies of the Sequence Listing, one on each of three compact discs are provided. Copy 1 and Copy 2 are identical. Copies 1 and 2 are also identical to the CRF. Each electronic copy of the Sequence Listing was created on November 20,2003 with a file size of 2373 KB. The file names are as follows: Copy 1-gl508901wo. txt; Copy 2-gl508901wo. txt; CRF-gl508901wo. txt.

BACKGROUND OF THE INVENTION [0003] The need for methods of assessing the toxic impact of a compound, pharmaceutical agent or environmental pollutant on a cell or living organism has led to the development of procedures which utilize living organisms as biological monitors. The simplest and most convenient of these systems utilize unicellular microorganisms such as yeast and bacteria, since they are the most easily maintained and manipulated. In addition, unicellular screening systems often use easily detectable changes in phenotype to monitor the effect of test compounds on the cell. Unicellular organisms, however, are inadequate models for estimating the potential effects of many compounds on complex multicellular animals, as they do not have the ability to carry out biotransformations.

[0004] The biotransformation of chemical compounds by multicellular organisms is a significant factor in determining the overall toxicity of agents to which they are exposed.

Accordingly, multicellular screening systems may be preferred or required to detect the toxic effects of compounds. The use of multicellular organisms as toxicology screening tools has been significantly hampered, however, by the lack of convenient screening mechanisms or endpoints, such as those available in yeast or bacterial systems.

Additionally, previous attempts to produce toxicology prediction systems have failed to provide the necessary modeling data and statistical information to accurately predict toxic responses (e. g., WO 00/12760, WO 00/47761, WO 00/63435, WO 01/32928, and WO 01/38579).

SUMMARY OF THE INVENTION [0005] The present invention is based on the elucidation of the global changes in gene expression in renal tissues or cells exposed to known toxins, in particular renal toxins, as compared to unexposed tissues or cells as well as the identification of individual genes that are differentially expressed upon toxin exposure.

[0006] In various aspects, the invention includes methods of predicting at least one toxic effect of a compound, predicting the progression of a toxic effect of a compound, and predicting the renal toxicity of a compound. The invention also includes methods of identifying agents that modulate the onset or progression of a toxic response. Also provided are methods of predicting the cellular pathways that a compound modulates in a cell. The invention also includes methods of identifying agents that modulate protein activities.

[0007] In a further aspect, the invention includes probes comprising sequences that specifically hybridize to genes in Tables 1-5N. In some instances, the genes are rat genes.

Also included are solid supports comprising at least two of the previously mentioned probes. The invention also includes a computer system that has a database containing information identifying the expression level in a tissue or cell sample exposed to a renal toxin of a set of genes comprising at least two genes in Tables 1-5N.

DETAILED DESCRIPTION [0008] Many biological functions are accomplished by altering the expression of various genes through transcriptional (e. g. through control of initiation, provision of RNA precursors, RNA processing, etc.) and/or translational control. For example, fundamental biological processes such as cell cycle, cell differentiation and cell death, are often characterized by the variations in the expression levels of groups of genes.

[0009] Changes in gene expression are also associated with the effects of various chemicals, drugs, toxins, pharmaceutical agents and pollutants on an organism or cell. For example, the lack of sufficient expression of functional tumor suppressor genes and/or the over expression of oncogene/protooncogenes after exposure to an agent could lead to tumorgenesis or hyperplastic growth of cells (Marshall (1991), Cell 64 : 313-326; Weinberg (1991), Science 254: 1138-1146). Thus, changes in the expression levels of particular genes (e. g. oncogenes or tumor suppressors) may serve as signposts for the presence and progression of toxicity or other cellular responses to exposure to a particular compound.

[0010] Monitoring changes in gene expression may also provide certain advantages during drug screening and development. Often drugs are screened for the ability to interact with a major target without regard to other effects the drugs have on cells. These cellular effects may cause toxicity in the whole animal, which prevents the development and clinical use of the potential drug.

[0011] The present inventors have examined tissue from animals exposed to known renal toxins which induce detrimental kidney effects, to identify global changes in gene expression induced by these compounds. These global changes in gene expression, which can be detected by the production of expression profiles (an expression level of one or more genes), provide useful toxicity markers that can be used to monitor toxicity and/or toxicity progression by a test compound. Some of these markers may also be used to monitor or detect various disease or physiological states, disease progression, drug efficacy, and drug metabolism.

Identification of Toxicity Markers [0012] To evaluate and identify gene expression changes that are predictive of toxicity, studies using selected compounds with well characterized toxicity have been conducted by the present inventors to catalogue altered gene expression. In the present studies, two different methods were used to create models and databases for predicting toxicity. In one model, RMA/PLS (raw data analysis by the robust multi-array average algorithm, with evaluation of predictive ability by the partial least squares algorithm), high doses of 39 compounds were selected as known renal toxins: acyclovir, adriamycin, amphotericin B, BEA (bromoethylamine hydrobromide), carboplatin, carbon tetrachloride, cephaloridine, chloroform, cidofovir, ciprofibrate, cisplatin, colchicine, cyclophosphamide, cyclosporine A, dantrolene, diflunisal, ethylene glycol, gentamicin, hexachloro-1, 3-butadiene, hydralazine, ifosfamide, indomethacin, lithium chloride, meloxicam, menadione, mercuric chloride, olsalazine, puromycin aminonucleoside, pentamidine, phenacetin, propyleneimine, semustine, sodium chromate, sodium oxalate, sulfadiazine, suramin, tacrolimus, thioacetamide and vancomycin. Low doses of these compounds, or the vehicles in which they were prepared, were used as negative controls. Eight additional compounds, or the vehicles in which they were prepared were also selected as negative controls: ceftazidime (a broad spectrum, beta-lactam antibiotic), 17-alpha-ethinylestradiol (a synthetic estrogen), gemfibrozil (a drug that lowers serum triglycerides and LDL cholesterol and increases HDL cholesterol), phenobarbital (a sedative and anticholinergic/antispasmodic drug), streptomycin (an aminoglycoside antibiotic), tamoxifen (an anti-estrogen, breast cancer drug), temozolomide (an anti-cancer drug, especially for brain tumors) and transplatin (an anti-tumor drug).

[0013] In the other model, MAS/LDA (raw data analysis by the Affymetrix MAS4 algorithm, with evaluation of predictive ability by linear discriminant analysis), high doses of the following compounds were selected as known renal toxins: indomethacin, diflunisal, colchicine, chloroform, diclofenac, menadione, sodium chromate, sodium oxalate, thioacetamide, vancomycin, acyclovir, adriamycin, AY-25329, bromoethylamine HBr (BEA), carboplatin, carbon tetrachloride, cephalosporine, cidofovir, cisplatin, citrinin, cyclophosphamide, cyclosporine, gentamicin, hexachloro-1, 3-butadiene, hydralazine, ifosfamide, lithium chloride, mercuric chloride, pamindronate, puromycin aminonucleoside (PAN), semustine and sulfadiazine. Negative controls include low doses of these compounds and the vehicles in which the compounds were prepared. Additional negative controls include the following compounds: captopril, ceftazidime, phenobrbital, streptomycin, tamoxifen, temozolomide and transplatin, as well as the vehicles in which they were prepared. In the MAS/LDA model the following vehicles were used: corn oil, methylcellulose, gum tragacanth and saline.

Rat Nephrotoxins [0014] Cephaloridine is an amphoteric, semi-synthetic, broad-spectrum cephalosporin derived from cephalosporin C. Cephalosporins are ß-lactam-containing antibiotics which prevent bacterial growth by inhibiting polymerization of the peptidoglycan bacterial cell wall. The linear glycan chains (composed of N-acetylglucosime and N-acetylmuramic acid) are cross-linked to each other by the coupling of short chains of several amino acids, the coupling resulting from the action of a transpeptidase. It is believed that cephalosporins act by blocking the activity of the transpeptidase (Goodman & Gilman's The Pharmalogical Basis of Therapeutics gth ed., J. G. Hardman et al. Eds. , McGraw Hill, New York, 1996, pp.

1074-1075,1089-1095).

[0015] Cephaloridine is administered intramuscularly and is used to treat infections of the respiratory tract, gastrointestinal tract and urinary tract, as well as infections of soft tissue, bones and joints. Noted adverse effects include hypersensitivity reactions (such as anaphylactic shock, urticaria and bronchospasm), gastrointestinal disturbances, candidiasis, and cardiovascular and blood toxicity, in particular, toxicity to the hematopoietic system (cells responsible for the formation of red and white blood cells and platelets).

[0016] Although cephaloridine may be nephrotoxic at high dosages, it is not as harmful to the kidneys as are the aminoglycosides and polymixins. High dosages of cephaloridine may cause acute renal tubular necrosis (Cecil Textbook of Medicine, 20th ed., part XII, p. 586, J.

C. Bennett and F. Plum Eds. , W. B. Saunders Co. , Philadelphia, 1996) or drug-induced interstitial nephritis, which is accompanied by elevated IgE levels, fever, arthralgia and maculopapular rash. Renal biopsopy demonstrates edema and interstitial inflammatory lesions, mainly with lymphocytes, monocytes, eosinophils and plasma cells. Vasculitis of small vessels may develop, leading to necrotising glomerulonephritis (G. Koren,"The nephrotoxic potential of drugs and chemicals. Pharmacological basis and clinical relevance.,"Med Toxicol Adverse Drug Exp 4 (1) : 59-72,1989).

[0017] Cephaloridine has also been shown to reduce mitochondrial respiration and uptake of anionic succinate and carrier-mediated anionic substrate transport (Tune et al. (1990), J Pharmacol Exp Ther 252: 65-69). In a study of oxidative stress and damage to kidney tissue, cephaloridine depleted reduced glutathione (GSH) and produced oxidized glutathione (GSSG) in the renal cortex. This drug also inhibited glutathione reductase and produced malondialdehyde and conjugated dienes (Tune et al. (1989), Biochem Pharmacol 38: 795-802). Because cephaloridine is actively transported into the proximal renal tubule, but slowly transported across the lumenal membrane into the tubular fluid, high concentrations can accumulate and cause necrosis. Necrosis can be prevented by administering inhibitors of organic anion transport, although such treatment may be counterproductive, as cephaloridine is passed in and out of the kidney by the renal organic anion transport system (Tune et al. (1980), Pharmacol Exp Ther 215: 186-190).

[0018] Cisplatin (Pt (NH3) 2 (CI) 2), a broad-spectrum anti-tumor agent, is commonly used to treat tumors of the testicles, ovaries, bladder, skin, head and neck, and lungs (PDR 47th ed., pp. 754-757, Medical Economics Co. , Inc. , Montvale, NJ, 1993; Goodman & Gilman's The Pharmalogical Basis of Therapeutics 9th ed., pp. 1269-1271, J. G. Hardman et al. Eds. , McGraw Hill, New York, 1996). Cisplatin diffuses into cells and functions mainly by alkylating the N of guanine, a highly reactive site, causing interstrand and intrastrand crosslinks in the DNA that are lethal to cells. The drug is not sensitive to the cell cycle, although its effects are most pronounced in S phase.

[0019] Because the drug is cleared from the body mainly by the kidneys, the most frequent adverse effect of cisplatin usage is nephrotoxicity, the severity of which increases with increasing dosage and treatment terms. Other adverse effects include renal tubule damage, myelosuppression (reduced numbers of circulating platelets, leukocytes and erythrocytes), nausea and vomiting, ototoxicity, serum electrolyte disturbances (decreased concentrations of magnesium, calcium, sodium, potassium and phosphate, probably resulting from renal tubule damage), increased serum concentrations of urea and creatinine, and peripheral neuropathies.

[0020] In one study on rats (Nonclercq et al. (1989), Exp Mol Pathol 51: 123-140) administration of cisplatin or carboplatin induced renal injury, carboplatin causing less damage than cisplatin. The most prominent injury was to the straight portion of proximal renal tubule.

[0021] In another rat study (Goldstein et al. (1981), Toxicol Appl Pharmacol 60: 163-175) animals injected with cisplatin displayed decreased food intake as drug dosage increased.

On day 2, the high-dose groups (10-15 mg/kg) exhibited a six or seven-fold elevation in BUN. On day 4, BUN elevation was noted in the 5mg/kg group. An increase in urine volume was observed beginning on days 3-4, along with decreased urine osmolality in the low-dose groups (2.5 or 5 mg/kg). Another experiment on rats (Agarwal et al. (1995), Kidney Int 48: 1298-1307) showed that cisplatin treatment produced elevations in serum creatinine levels, which began on day 3 and progressed for the duration of the study.

[0022] Puromycin aminonucleoside (PAN, C22H29N705), an antibiotic produced by Streptomyces alboniger, inhibits protein synthesis and is commonly used experimentally on rats to mimic human minimal change disease. One study showed that PAN-injected rats demonstrated an increase in levels of serum non-esterified fatty acids, while the serum albumin concentration was negatively affected (Sasaki et al. (1999), Adv Exp Med Biol 467: 341-346).

[0023] In another rat study, an adenosine deaminase inhibitor prevented PAN nephrotoxicity, indicating that PAN toxicity is linked to adenosine metabolism (Nosaka et al. (1997), Free Radic Biol Med 22: 597-605). Another group showed that PAN, when administered to rats, led to proteinuria, a condition associated with abnormal amounts of protein in the urine, and renal damage, e. g. blebbing of glomerular epithelial cells, focal separation of cells from the glomerular basement membrane, and fusion of podocytes (Olson et al. (1981), Lab Invest 44 : 271-279). In another study on rats, administration of PAN induced glomerular epithelial cell apoptosis in a dose-and time-dependent manner (Sanwal et al. (2001), Exp Mol Pathol 70 : 54-64).

[0024] One study with PAN-injected rats (Koukouritaki et al. (1998), JInvestigMed 46 : 284-289) examined the changes in the expression of the proteins paxillin, focal adhesion kinase, and Rho, all of which regulate cell adhesion to the extracellular matrix. Paxillin levels increased steadily, peaked at day 9 after PAN injection, and then remained elevated even after proteinuria resolved. There was no observed change in expression of either focal adhesion kinase or Rho.

[0025] BEA, (C2H6BrN. HBr), is commonly used experimentally on rats to induce papillary necrosis and renal cortex damage, which is similar to human analgesic nephropathy. BEA- induced papillary necrosis in rats eventually leads to the onset of focal glomerular sclerosis and nephrotic proteinuria (Garber et al. (1999), Am JKidney Dis 33: 1033-1039). Even at low doses (50 mg/kg), BEA can induce an apex limited renal papillary necrosis (Bach et al.

(1983), Toxicol Appl Pharmacol 69 : 333-344). In male Wistar rats, BEA administered at 100 mg/kg was shown to cause renal papillary necrosis within 24 hours (Bach et al. (1991), Food Chem Toxicol 29: 211-219). Additionally, Bach et al. showed that there was an increase in urinary triglycerides, and lipid deposits were seen by Oil Red O lipid staining in the cells of the collecting ducts and hyperplastic urothelia adjacent to the necrosed region.

[0026] It has also been shown that succinate and citrate concentrations are significantly lower in the urine of BEA-treated rats (Holmes et al. (1995), Arch Toxicol 70 : 89-95).

Moreover, BEA treatment induced glutaric and adipic aciduria, which is symptomatic of an enzyme deficiency in the acyl CoA dehydrogenases. The same study examined urinary taurine levels in desert mice, and in BEA-treated desert mice there was an increase in the urinary taurine level which is indicative of liver toxicity.

[0027] Another study on BEA-treated rats showed that there was an increase in the concentrations of creatine in the renal papilla and glutaric acid in the liver, renal cortex, and renal medulla as soon as 6 hours post-treatment (Garrod et al. (2001), Magn Reson Med 45: 781-790).

[0028] Discovered and purified in the early 1960's, gentamicin is a broad-spectrum aminoglycoside antibiotic that is cidal to aerobic gram-negative bacteria and commonly used to treat infections, e. g. , those of the urinary tract, lungs and meninges. As is typical for an aminoglycoside, the compound is made of two amino sugar rings linked to a central aminocyclitol ring by glycosidic bonds. Aminoglycosides are absorbed poorly with oral administration, but are excreted rapidly by the kidneys. As a result, kidney toxicity is the main adverse effect, although ototoxicity and neuromuscular blockade can also occur.

Gentamicin acts by interfering with bacterial protein synthesis. This compound is more potent than most other antibacterial inhibitors of protein synthesis, which are merely bacteriostatic, and its effects on the body are, likewise, more severe (Goodman & Gilman's The Pharmalogical Basis of Therapeutics 9th ed., pp. 1103-1115, J. G. Hardman et al. Eds. , McGraw Hill, New York, 1996).

[0029] Aminoglycosides work rapidly, and the rate of bacterial killing is concentration- dependent. Residual bactericidal activity remains after serum concentration has fallen below the minimum inhibitory concentration (MIC), with a duration that is also dosage/concentration-dependent. The residual activity allows for once-a-day administration in some patients. These drugs diffuse into bacterial cells through porin channels in the outer membrane and are then transported across the cytoplasmic membrane via a membrane potential that is negative on the inside (Goodman & Gilman, supra).

[0030] Kidney damage, which can develop into renal failure, is due to the attack of gentamicin on the proximal convoluted tubule, particularly in the S 1 and S2 segments. The necrosis, however, is often patchy and focal (Shanley et al. (1990), Ren Fail 12: 83-87). A rat study by Shanley et al. showed that superficial nephrons are more susceptible to necrosis than juxtamedullary nephrons, although the initial segment of the superficial nephrons is remarkably resistant to necrosis.

[0031] Reported enzymatic changes upon gentamicin treatment are increased activities of N-acetyl-beta-D-glucosaminidase and alkaline phosphatase and decreased activities of sphingomyelinase, cathepsin B, Na+/K+-ATPase, lactate dehydrogenase and NADPH cytochrome C reductase, along with decreased protein synthesis and alpha-methylglucose transport (Monteil et al. (1993), Ren Fail 15: 475-483). An increase in gamma-glutamyl transpeptidase activity in urine has also been reported (Kocaoglu et al. (1994), Arch Immunol Ther Exp (Warsz) 42: 125-127), and the quantification of this enzyme in urine is a useful marker for monitoring gentamicin toxicity.

[0032] One source of renal pathology resulting from gentamicin treatment is the generation of reactive oxygen metabolites. Gentamicin has been shown, both in vitro and in vivo, to be capable of enhancing the production of reactive oxygen species. Iron, a necessary co-factor that catalyzes free-radical formation, is supplied by cytochrome P450 (Baliga et al. (1999), Drug Metab Rev 31: 971-997).

[0033] A gene delivery experiment in rats, in which the human kallikrein gene was cloned into an adenovirus vector and the construct then co-administered with a gentamicin preparation, showed that kallikrein can protect against gentamicin-induced nephrotoxicity.

Significantly increased renal blood flow, glomerular filtration rates and urine flow were observed, along with decreased renal tubular damage, cellular necrosis and lumenal protein casts. Kallikrein gene delivery also caused a decrease in blood urea nitrogen levels and increases in urinary kinin and nitrite/nitrate levels. This study provides evidence that the tissue kallikrein-kinin system may be a key pathway that is perturbed during the induction of nephrotoxicity by gentamicin (Murakami et al. (1998), Kidney Int 53: 1305-1313).

[0034] Ifosfamide, an alkylating agent, is commonly used in chemotherapy to treat testicular, cervical, and lung cancer. Ifosfamide is slowly activated in the liver by hydroxylation, forming the triazene derivative 5- (3, 3-dimethyl-l-triazeno)-imidazole-4- carboxamide (DTIC) (Goodman & Gilman's The Pharmacological Basis of Therapeutics glh ed., p. 1235, J. G. Hardman et al., Eds. , McGraw Hill, New York, 1996). Cytochrome P450 activates DTIC via an N-demethylation reaction yielding an alkylating moiety, diazomethane. The active metabolites are then able to cross-link DNA causing growth arrest and cell death. Though ifosfamide is therapeutically useful, it is also associated with nephrotoxicity, urotoxicity, and central neurotoxicity.

[0035] Mesna, another therapeutic, is often administered concomitantly to prevent kidney and bladder problems from arising (Brock and Pohl (1986), IARC Sci Publ 78 : 269-279).

However, there are documented cases in which tubular toxicity occurred and elevated urinary levels of alanine aminopeptidase and N-acetyl-beta-D-glucosaminidase were found in patients even though mesna was administered alongside ifosfamide (Goren et al. (1987), Cancer Treat Rep 71: 127-130).

[0036] One study examined 42 patients that had been administered ifosfamide to treat advanced soft-tissue sarcoma (Stuart-Harris et al. (1983), Cancer Chemother Pharmacol 11: 69-72). The ifosfamide dosage varied from 5.0 g/m2 to 8.0 g/m2, and all of the patients were given mesna to counteract the negative effects of ifosfamide. Even so, nausea and vomiting were common to all of the patients. Out of the 42 patients, seven developed nephrotoxicity, and two of the cases progressed to fatal renal failure.

[0037] In another clinical study, renal tubular function was monitored in 18 neuroblastoma patients (Caron et al. (1992), Med Pediatr Oncol 20: 42-47). Tubular toxicity occurred in at least 12 of the patients, and seven of those patients eventually developed Debre-de Toni- Fanconi syndrome, although in 3 cases the syndrome was reversible.

[0038] Fanconi syndrome is a disorder marked by dysfunction of the proximal tubules of the kidney. It is associated with aminoaciduria, renal glycosuria, and hyperphosphaturia.

Ifosfamide is often used experimentally on rats to induce Fanconi syndrome. In one study, rats that were administered 80 mg/kg of ifosfamide had significantly lower body weight and hematocrit than control rats (Springate and Van Liew (1995), JAppl Toxicol 15 : 399-402).

Additionally, the rats had low-grade glucosuria, proteinuria, and phosphaturia. In a mouse study, ifosfamide induced elevated serum creatinine and urea levels and decreased the clearance rate of creatinine (Badary (1999), JEthnopharmacol 67: 135-142).

[0039] Cyclophosphamide, a nitrogen mustard and alkylating agent, is highly toxic to dividing cells and is commonly used in chemotherapy to treat malignant lymphomas, such as non-Hodgkin's lymphomas and Burkitt's lymphom, multiple myeloma, leukemias, neuroblastomas, ovarian adenocarcinomas and retinoblastomas, as well as breast and lung cancer (Goodman & Gilman's The Pharmacological Basis of Therapeutics 9th ed., pp. 1234, 1237-1239, J. G. Hardman et al., eds. , McGraw Hill, New York, 1996; Physicians Desk Reference, 47th ed. , pp. 744-745, Medical Economics Co. , Inc. , Montvale, NJ, 1993).

Additionally, cyclophosphamide is used as an immunosuppressive agent in bone marrow transplantation and following organ transplantation. Although cyclophosphamide is therapeutically useful against certain types of cancer, it is also associated with cardiotoxicity, nephrotoxicity (including renal tubular necrosis), hemorrhagic cystitis, myelosuppression, hepatotoxicity, impairment of male and female reproductive systems, interstitial pneumonitis and central nervous system toxicity. l0040] Once in the liver, cyclophosphamide is hydroxylated by the cytochrome P450 mixed function oxidase system, producing the active metabolites phosphoramide mustard and acrolein, which cross-link DNA and cause growth arrest and cell death. These metabolites, however, are highly toxic and cause adverse effects in the other organs into which they are transported, such as the kidneys. Acrolein is removed from the kidneys by secretion into the urine, resulting in cystitis (inflammation of the bladder), often hemorrhagic cystitis.

[0041] In the kidney, cyclophosphamide induces necrosis of the renal distal tubule.

Cyclophosphamide, which is structurally similar to the anti-cancer drug ifosfamide, does not induce damage to the renal proximal tubule nor does it induce Debre-de Toni-Fanconi syndrome (Rossi et al. (1997), Nephrol Dial Transplant 12: 1091-1092).

[0042] One clinical trial of patients being treated with cyclophosphamide showed that renal damage from the drug leads to a reduced biotransformation rate and low renal clearance of the drug, resulting in a build-up of toxic alkylating metabolic products (Wagner et al.

(1980), Arzneimittelforschung 30: 1588-1592).

[0043] In a study of patients suffering from malignant lymphomas and mammary carcinomas, a direct relationship was found between the dose of cyclophosphamide used in treatment and the concentration of alkylating metabolites in the patients'urine. The upper limit of the dose was determined by the nature and degree of the toxic side effects, rather than by the rate at which the drug could be metabolized (Saul et al. (1979), J Cancer Res Clin Oncol 94: 277-286). It is the acrolein itself that is toxic, not the alkylating activity of cyclophosphamide (Brock et al. (1979), Arzneimittelforschung 29: 659-661). A study on rats also showed that acrolein from the kidneys can produce hemorrhagic cystitis and that the acrolein concentration is directly related to the frequency and severity of the cystitis (Chijiwa et al. (1983), Cancer Res 43 : 5205-5209).

[0044] Carboplatin, a platinum coordination complex, is commonly used in chemotherapy as an anti-tumor agent. As a chemotherapeutic agent, carboplatin acts similarly to cisplatin.

Carboplatin enters the cell by diffusion where it is activated by hydrolysis (Goodman & Gilman's The Pharmacological Basis of Therapeutics 9th ed., p. 1270-1271, J. G. Hardman et al. Eds. , McGraw Hill, New York 1996). Once activated, the platinum complexes are able to react with DNA causing cross-linking to occur. One of the differences between carboplatin and cisplatin is that carboplatin is better tolerated clinically. Some of the side- effects associated with cisplatin, such as nausea, neurotoxicity, and nephrotoxicity, are seen at a lesser degree in patients administered carboplatin. Some other side-effects are hypomagnesaemia and hypokalaemia (Kintzel (2001), Drug Saf 24 : 19-38).

[0045] In one study on male Wistar rats, carboplatin was administered at a dosage of 65mg/kg (Wolfgang et al. (1994), Fundam Appl Toxicol 22 : 73-79). After treatment with carboplatin, CGT excretion was increased approximately two-fold.

[0046] Another study compared cisplatin and carboplatin when given in combination with vindesine and mitomycin C (Jelic et al. (2001) Lung Cancer 34: 1-13). The study showed that carboplatin administered with vindesine and mitomycin C was advantageous in terms of overall survival, although the regimen was more hematologically toxic than when cisplatin was given.

[0047] AY-25329, is a phenothiazine that has been shown to be mildly hepatotoxic and to induce nephrosis. Its structure is shown below.

[0048] Phenothiazines are a class of psychoactive drugs. They have been used to treat schizophrenia, paranoia, mania, hyperactivity in children, some forms of senility, and anxiety (http ://www. encyclopedia. com/articlesnew/36591. html). Some side effects associated with prolonged use of the drugs are reduced blood pressure, Parkinsonism, reduction of motor activity, and visual impairment.

[0049] Chlorpromazine (Thorazine or Largactil) is an aliphatic phenothiazine and is widely used for treating schizophrenia and manic depression. Prolactin secretion is increased while taking chlorpromazine, and galactorrhea and gynecomastia have both been associated with the drug (http://www. mentalhealth. com/drug/p30-cOl. html). Trifluoperazine is another prescribed phenothiazine. It is used to treat anxiety, to prevent nausea and vomiting, and to manage psychotic disorders (http://www. mentalhealth. com/ drug/p30-sO4. html). Negative side-effects that have been associated with the drug are liver damage, bone marrow depression, and Parkinsonism.

[0050] Acyclovir (9- [ (2-hydroxyethyl) methyl] guanine, Zovirax (E)), an anti-viral guanosine analogue, is used to treat herpes simplex virus (HSV), varicella zoster virus (VZV) and Epstein-Barr virus (EBV) infections. It is transported into cells by the nucleoside transporter that imports guanine, and acyclovir is phosphorylated by virally encoded thymidine kinase (TK). Other kinases convert acyclovir to its activated di-and triphosphate forms, which prevent the polymerization of viral DNA. Acyclovir triphosphate competes with dGTP for the viral polymerase, and acyclovir is preferentially incorporated, but as a monophosphate. As a result, chain elongation ceases (Fields Virology 3d ed., Fields et al., eds. , pp. 436-440, Lippincott-Raven Publishers, Philadelphia, 1996; Cecil Textbook of Medicine, 20"'cd., part XII, p. 1742, J. C. Bennett and F. Plum Eds. , W. B. Saunders Co., Philadelphia, 1996).

[0051] The pharmacokinetics of acyclovir show that it has a useful half-life of about three hours and that most of it is excreted in the urine largely unchanged (Brigden et al. (1985), Scand JInfect Dis Suppl 47 : 33-39). Not surprisingly, the most frequent adverse effect of acyclovir treatment is damage to various parts of the kidney, particularly the renal tubules.

Crystalluria, or the precipitation of crystals (in this case, crystals of acyclovir), in the lumina of the renal tubules can occur (Fogazzi (1996), Nephrol Dial Transplant 11: 379-387). If the drug crystallizes in the renal collecting tubules, obstructive nephropathy and tubular necrosis can result (Richardson (2000), Vet Hum Toxicol 42 : 370-371). Tissues from biopsies of affected patients showed dilation of the proximal and distal renal tubules, with loss of the brush border, flattening of the lining cells and focal nuclear loss (Becker et al.

(1993), Am JKidney Dis 22: 611-615).

[0052] Citrinin, a mycotoxin produced by the fungus Penicillium citrinum, is a natural contaminant of foods and feeds (Bondy and Armstrong (1998) Cell Biol. Toxicol. 14: 323- 332). It is known that mycotoxins can have negative effects on the immune system, however citrinin-treated animals have been shown to stimulate responses against antigens (Sharma (1993) J. Dairy Sci. 76: 892-897). Citrinin is a known nephrotoxin, and in birds such as chickens, ducklings, and turkeys, it causes diarrhea, increased food consumption and reduced weight gain due to kidney degeneration (Mehdi et al. (1981) Food Cosmet.

Toxicol. 19: 723-733; Mehdi et al. (1984) Vet. Pathol. 21: 216-223). In the turkey and duckling study, both species exhibited nephrosis with the occurrence of hepatic and lymphoid lesions (Mehdi et al., 1984).

[0053] In one study, citrinin was administered to rabbits as a single oral dose of either 120 or 67 mg/kg (Hanika et al. (1986) Vet. Pathol. 23: 245-253). Rabbits treated with citrinin exhibited renal alterations such as condensed and distorted mitochondria, distended intercellular spaces of the medullary and straight cortical distal tubules, and disorganization of interdigitating processes. In another rabbit study, citrinin-administered rabbits displayed azotaemia and metabolic acidosis (Hanika et al. (1984) Food Chem. Toxicol. 22: 999-1008).

Renal failure was indicated by decreased creatinine clearance and increased blood urea nitrogen and serum-creatinine levels.

[0054] In the past, mercury was an important component of pharmaceuticals, particularly of antiseptics, antibacterials, skin ointments, diuretics and laxatives. Although, mercury has been largely replaced by more effective, more specific and safer compounds, making drug- induced mercury poisoning rare, it is still widely used in industry. Poisoning from occupational exposure and environmental pollution, such as mercury release into public water supplies, remains a concern as wildlife, domestic animals and humans are affected.

[0055] Because of their lipid solubility and ability to cross the blood-brain barrier, the most dangerous form of mercury is the organomercurials, the most common of which is methylmercury, a fungicide used for disinfecting crop seeds. In a number of countries, incidents involving large-scale illness and death from mercury poisoning have been reported when mercury-contaminated seeds were planted and the crops harvested and consumed. A second source of organic mercury poisoning results from industrial chemicals containing inorganic mercury, such as mercury catalysts, which form methylmercury as a reaction product. If this waste product is released into reservoirs, lakes, rivers or bays, the surrounding population can become sick or die, particularly those who eat local fish.

[0056] The inorganic salt mercuric chloride, HgClz, as well as other mercuric salts, are more irritating and more toxic than the mercurous forms. Mercuric chloride is used today in industry, for the manufacture of bleach, electronics, plastics, fungicides and dental amalgams. The main source of human exposure is industrial dumping into rivers (Goodman & Gilman's : The Pharmacological Basis of Therapeutics (9th ed. ), pp. 1654-1659, McGraw- Hill, New York, 1996).

[0057] When inorganic mercury salts are ingested, about 10% of the mercuric ions are absorbed by the gastrointenstinal tract, and a considerable portion of the Hg2+ can remain bound to the mucosal surfaces. The highest concentration of Hg2+ is found in the kidneys, as it is retained there longer than in other tissues. Consequently, the kidneys are the organ most adversely affected by inorganic mercury poisoning. The proximal tubules are the major site of damage, where tubular necrosis results. The mercury affects primarily the S2 and S3 portions of the proximal tubules, but, at high levels of mercury exposure, the S 1 and distal portions of the tubules are also damaged. These regions of the nephrons are affected because they contain enzymes (such as gamma-glutamyltranspeptidase) and transport proteins (such as the basolateral organic anion transport system) involved in mercury uptake (Diamond et al. (1998), Toxicol Pathol 26 : 92-103).

[0058] Urinary markers of mercury toxicity which can be detected in NMR spectra include elevated levels of lactate, acetate and taurine and decreased levels of hippurate (Holmes et al. (2000), Chem Res Toxicol 13 : 471-478). Known changes in gene expression in kidneys exposed to Hg2+ include up-regulation of the heat-shock protein hsp72 and of the glucose- regulated protein grp94. The degree of tissue necrosis and level of expression of these proteins is proportional to both the dose of mercury (Hg2+) and the length of the exposure time to mercury (Hg2+), with hsp72 accumulating in the renal cortex and grp94 accumulating in the renal medulla (Goering et al. (2000), Toxicol Sci 53: 447-457).

[0059] Indomethacin is a non-steroidal antiinflammatory, antipyretic and analgesic drug commonly used to treat diseases such as rheumatoid arthritis, osteoarthritis, ankylosing spondylitis and gout. This drug acts as a potent inhibitor of prostaglandin synthesis; it inhibits the cyclooxygenase enzyme necessary for the conversion of arachidonic acid to prostaglandins (PDR 47th ed., Medical Economics Co. , Inc. , Montvale, NJ, 1993; Goodman & Gilman's The Pharmalogical Basis of Therapeutics 9th ed., J. G. Hardman et al., Eds. , McGraw Hill, New York, 1996, pp. 1074-1075,1089-1095 ; Cecil Textbook of Medicine, 20th ed. , part XII, pp. 772-773,805-808, J. C. Bennett and F. Plum Eds. , W. B. Saunders Co. , Philadelphia, 1996).

[0060] The most frequent adverse effects of indomethacin treatment are gastrointestinal disturbances, e. g., bleeding, ulcers and perforations, although renal toxicity can also result, particularly after long-term administration. In rats, hemorrhage and necrosis have been observed in the renal papillae and fornix, as well as damage to the thick ascending limbs (mTALs), and interstitial nephritis with hematuria, proteinuria and nephrotic syndrome have been reported in humans. Patients suffering from renal dysfunction risk developing a reduction in renal blood flow and urinary outflow, because renal prostaglandins play an important role in renal perfusion and glomerular filtration (Heyman et al. (1997), Kidney Int 51 : 653-663).

[0061] Diflunisal, a non-steroidal anti-inflammatory drug (NSAID), is a difluorophenyl derivative of salicylic acid (Goodman & Gilman's The Pharmacological Basis of Therapeutics 9th ed., p. 631, J. G. Hardman et al., Eds. , McGraw Hill, New York, 1996). It is most frequently used in the treatment of osteoarthritis and musculoskeletal strains.

NSAIDs have analgesic, antipyretic and anti-inflammatory actions, however hepatotoxicity is known to be an adverse side effect of NSAID treatment (Masubuchi et al. (1998). I.

Pharmacol. Exp. Ther. 287: 208-213). Diflunisal has been shown to be less toxic than other NSAIDs, nevertheless over long periods of dosage it can lead to deleterious effects on platelet or kidney function (Bergamo et al. (1989) Am. J. Nephrol. 9: 460-463). Other side effects that have been associated with diflunisal treatment are diarrhea, dizziness, drowsiness, gas or heartburn, headache, nausea, vomiting, and insomnia (http://arthritisinsight. com/medical/meds/dolobid. html).

[0062] Masubuchi et al. compared the hepatotoxicity of 18 acidic NSAIDs. In the study, diflunisal (administered at a concentration of 500 uM) was shown to increase LDH leakage in rat hepatocytes, a marker for cell injury, when compared to the control sample. In addition, treatment with diflunisal led to decreased intracellular ATP concentrations.

[0063] One study compared the effects of diflunisal and ibuprofen when given to patients over a two week period (Muncie and Nasrallah (1989) Clin. Ther. 11: 539-544). In both the ibuprofen and the diflunisal group, two patients complained of abdominal cramping. The study indicated that even during short-term usage some gastrointestinal effects may occur.

The toxic dose used in this study was chosen as one that did not induce significant gastric ulceration in rats. The group of rats given the high dosage of diflunisal had increased concentrations of creatinine which is consistent with renal injury, although dehydration may also cause increases in creatinine concentration.

[0064] Cidofovir (Vistide (g)) is an antiviral cytosine analog used in the treatment of viral infections such as herpesvirus, adenovirus, papillomavirus, poxvirus and hepadnavirus (Goodman & Gilman's The Pharmacological Basis of Therapeutics 9th ed., p. 1216, J. G.

Hardman et al., Eds. , McGraw Hill, New York, 1996). It is also useful for the treatment of cytomegalovirus (CMV) infection, which is a type of herpesvirus.

[0065] Some mild side effects seen in patients receiving cidofovir are nausea, vomiting, and fever. The most serious reported side effect of the drug is kidney toxicity (http://tthivclinic. com/cido. html). In response to the threat of nephrotoxicity, it is necessary for patients receiving cidofovir to have their kidneys checked before treatment, and the patients must be monitored during treatment for early symptoms of kidney problems. In addition, cidofovir is given with fluids to help reduce the risk of kidney toxicity (http ://www. aidsinfonyc. org/ network/simple/cido. html). Probenecid, a drug that helps protect the kidneys, is normally administered concomitantly (Lalezari and Kuppermann (1997) J. Acquir. Immune Defic.

Syndr. Hum. Retrovirol. 14: S27-31).

[0066] One study compared the safety and efficacy of cidofovir in the treatment of CMV (Lalezari et al. (1998) J. Acquir. Immune Defic. Syndr. Hum. Retrovirol. 17: 339-344).

Approximately 40% of the patients exhibited dose-dependent asymptomatic proteinuria and 25% of the patients had elevated serum creatinine levels.

[0067] Pamidronate (Aredia@) is a bisphosphonate drug that is clinically used to inhibit bone resorption and make bones more stable. It is used to treat hypercalcemia (too much calcium in the blood) that occurs with some types of cancer. Typically administered by intravenous injection, pamidronate is frequently used in patients with breast cancer or multiple myeloma whose disease has spread to the bones. Some side effects related to pamidronate treatment are abdominal cramps, chills, confusion, fever, muscle spasms, nausea, muscle stiffness, and swelling at the injection site (http ://www. nursing. uiowa. edu/sites/PedsPain/Adjuvants/PAMIDRnt. html). Patients with kidney problems may be prohibited from using pamidronate as it is excreted through the kidneys.

[0068] In one study, rats and mice were given varying doses of labeled pamidronate (Cal and Daley-Yates (1990) Toxicology 65: 179-197). Pamidronate treatment led to significant weight loss and a decrease in creatinine clearance. Morphological studies showed a loss of brush border membranes and the presence of focal proximal tubular necrosis.

[0069] Another study compared the tolerability of different treatments for hypercalcemia of malignancy by reviewing articles published between 1979 and 1998 (Zojer et al. (1999) Drug Saf 21: 389-406). The authors found that elevated serum creatinine level, nausea, and fever were reported following treatment with bisphosphonates such as pamidronate.

[0070] Markowitz et al. (2001, J. Am. Soc. Nephrol. 12: 1164-1172) tried to determine whether there was a correlation between pamidronate treatment and collapsing focal segmental glomerulosclerosis (FSGS). The authors examined the histories of seven patients who had developed collapsing FSGS, and they found that the only drug treatment in common was the administration of pamidronate. When given at the recommended dose of 90 mg per month, renal toxicity was rare. However, when pamidronate was given at higher doses nephrotoxicity occurred.

[0071] Lithium, an alkali metal, is the main pharmacological treatment for bipolar disorders. It is typically given as a salt, such as lithium carbonate or lithium citrate. Some common side effects of lithium treatment are an increase in urination, increase in drinking, dry mouth, weight gain, fine tremor, and fatigue. Some more serious side effects related to lithium treatment are blurred vision, mental confusion, seizures, vomiting, diarrhea, muscle weakness, drowsiness, and coarse tremor (Goodman & Gilman's The Pharmacological Basis of Therapeutics glh ed. , p. 448, J. G. Hardman et al., Eds. , McGraw Hill, New York, 1996).

[0072] Since lithium is often used on a maintenance basis for a lifelong period, numerous studies have been performed to try and elucidate the effects of lithium on the kidney. One group administered lithium in daily doses within the human therapeutic range to male Wistar rats (Kling et al. (1984) Lab Invest 50: 526-535). Rats that were given lithium developed marked polyuria within three weeks of the initial dosing. The rats displayed elevated free water clearance and vasopressin-resistant diabetes insipidus. The cortical collecting tubules displayed morphological changes, e. g. dilation of the tubules, bulging cells lining the tubules, enlarged nuclei, following lithium treatment.

[0073] Another study examined a human population that had been given lithium for the treatment of bipolar disorder (Markowitz et al. (2000) J. Am. Soc. Nephrol. 11: 1439-1448).

The patients had a mean age of 42.5 years and had been undergoing lithium treatment from 2 to 25 years (mean of 13.6 years). Approximately one fourth of the patients had nephrotic proteinuria, almost 90% of them had nephrogenic diabetes insipidus (NDI), and renal biopsies revealed a chronic tubulointerstitial nephropathy in all of the patients. Following cessation of lithium treatment, seven of the patients proceeded to end-stage renal disease.

[0074] Even though nephrotoxicity is a known side effect of lithium treatment, some studies have indicated that in actuality it is not all that common (Johnson (1998) Neuropsychopharmacology 19: 200-205). One study showed that the NDI-like effect in lithium treatment was easily overcome by increasing the levels of arginine vasopressin (AVP) (Carney et al. (1996) Kidney Int 50: 377-383). Other studies have suggested that patients with psychiatric disorders display certain defects in renal function without undergoing lithium treatment (Gitlin (1999) Drug Saf 20 : 231-243).

[0075] Hydralazine, an antihypertensive drug, causes relaxation of arteriolar smooth muscle. Such vasodilation is linked to vigorous stimulation of the sympathetic nervous system, which in turn leads to increased heart rate and contractility, increased plasma renin activity, and fluid retention (Goodman & Gilman's The Pharmacological Basis of Therapeutics 9th ed., p. 794, J. G. Hardman et al., Eds. , McGraw Hill, New York, 1996).

The increased renin activity leads to an increase in angiotensin II, which in turn causes stimulation of aldosterone and sodium reabsorption.

[0076] Hydralazine is used for the treatment of high blood pressure (hypertension) and for the treatment of pregnant women suffering from high blood pressure (pre-eclampsia or eclampsia). Some common side effects associated with hydralazine use are diarrhea, rapid heartbeat, headache, decreased appetite, and nausea. Hydralazine is often used concomitantly with drugs that inhibit sympathetic activity to combat the mild pulmonary hypertension that can be associated with hydralazine usage.

[0077] In one hydralazine study, rats were fed hydralazine and mineral metabolism was monitored (Peters et al. (1988) Toxicol Lett 41: 193-202). Manganese and zinc concentrations were not effected by hydralazine treatment, however tissue iron concentrations were decreased and kidney copper concentrations were increased compared to control groups.

[0078] Another study compared the effects of hydrazine, phenelzine, and hydralazine treatment on rats (Runge-Morris et al. (1996) Drug Metab Dispos 24: 734-737).

Hydralazine caused an increase in renal GST-alpha subunit expression, although unlike hydrazine and phenelzine it did not alter renal cytochrome P4502E1 expression.

[0079] Colchicine, an alkoloid of Colchicum autumale, is an antiinflammatory agent used in the treatment of gouty arthritis (Goodman & Gilman's The Pharmacological Basis of Therapeutics 9th ed., p. 647, J. G. Hardman et al., Eds. , McGraw Hill, New York, 1996).

[0080] An antimitotic agent, colchicine binds to tubulin which leads to depolymerization and disappearance of the fibrillar microtubules in granulocytes and other motile cells. In doing so, the migration of granulocytes into the inflamed area is inhibited. Through a series of events, the inflammatory response is blocked.

[0081] Some common, mild side effects associated with colchicine treatment are loss of appetite and hair loss. More severe side effects that warrant cessation of treatment are nausea, vomiting, diarrhea, and abdominal pain. Colchicine overdose can induce multiorgan failure with a high incidence of mortality. In this setting, renal failure is multifactorial and related to prolonged hypotension, hypoxemia, sepsis, and rhabdomyolysis. In rats, less dramatic doses have been shown to inhibit the secretion of many endogenous proteins such as insulin and parathyroid hormone.

[0082] One study investigated the effects of colchicine on microtubule polymerization status and post-translational modifications of tubulin in rat seminiferous tubules (Correa and Miller (2001) Biol Reprod 64: 1644-1652). Colchicine caused extensive microtubule depolymerization, and total tubulin levels decreased twofold after colchicine treatment. The authors also found that colchicine treatment led to a decrease in tyrosination of the microtubule pool of tubulin which was associated with depolymerization of microtubules.

[0083] Sulfadiazine, a sulfonamide, is an antimicrobial agent. It is commonly used concomitantly with pyrimethamine to treat toxoplasmosis, an infection of the brain, in patient suffering from AIDS. These drugs are able to cross the blood-brain barrier and are used at relatively high doses. In addition, sulfadiazine has been shown to be effective at preventing certain types of meningococcal diseases and in treating urinary tract infections.

[0084] Sulfonamides in general are structural analogs of para-aminobenzoic acid (PABA).

Because they are competitive antagonists of PABA, sulfonamides are effective against bacteria that are required to utilize PABA for the synthesis of folic acid (Goodman & Gilman's The Pharmacological Basis of Therapeutics glh ed., p. 1058-1060, J. G. Hardman et al., Eds. , McGraw Hill, New York, 1996).

[0085] The main side effects associated with sulfadiazine treatment are fever and skin rashes. Decreases in white blood cells, red blood cells, and platelets, nausea, vomiting, and diarrhea are some other side effects that may result from sulfadiazine treatment. The most troublesome problem with this drug for HIV/AIDS patients is kidney toxicity. These patients tend to use these drugs for extended periods of time, which puts a constant strain on the kidneys. In addition, kidney stones tend to form in the bladder and ureter thereby blocking the flow of urine. Kidney damage may result, and if left untreated kidney failure may occur. Therefore, patients being treated with sulfadiazine are instructed to increase their fluid intake in order to prevent crystal formation in the kidneys.

[0086] One case study examined four HIV-positive patients who had been given sulfadiazine to treat toxoplasmosis (Crespo et al. (2000) Clin Nephrol 54 : 68-72). All four of the patients, one of whom was a previously healthy person, developed oliguria, abdominal pain, renal failure, and displayed multiple radiolucent renal calculi in echography. Following extensive hydration and alcalinization, the renal function of the patients returned to normal.

[0087] Adriamycin, known generically as doxorubicin, is an anthracycline antibiotic produced by the fungus Streptomyces peucetius. It is an anti-tumor drug used in the treatment of breast, ovarian, bladder, and lung cancers as well as non-Hodgkin's lymphom, Hodgkin's disease and sarcoma (Goodman & Gilman's The Pharmacological Basis of Therapeutics glh ed., p. 1264-1265, J. G. Hardman et al., Eds. , McGraw Hill, New York, 1996).

[0088] Adriamycin has tetracycline ring structures with the sugar daunosamine attached by glycosidic linkage. It is able to intercalate with DNA, it affects DNA and RNA synthesis, and it can interact with cell membranes and alter their functions. Typically the drug is cell- cycle specific for the S phase of cell division. By binding to the cancer cells'DNA and blocking topoisomerase II, cancer cells are unable to divide and grow.

[0089] Some common side effects associated with adriamycin treatment are fatigue, a drop in white blood cell, red blood cell, or platelet count, hair loss, skin discoloration, and watery eyes (www. cancerhelp. org. uk/help/default. asp? page=4025). More serious side effects include myocardial toxicity, ulceration and necrosis of the colon, and development of a second cancer.

[0090] Because of its utility in fighting cancer, numerous studies have been performed in attempts to further understand the mechanisms and effects of adriamycin. In one study, investigators injected mice with a single dose of adriamycin (Chen et al. (1998) Nephron 78: 440-452). The mice exhibited signs of combined glomerular albuminuria and immunoglublinuria, progressively elevated levels of nitrite/nitrate in the urine, abnormal renal function, and other symptoms indicative of focal segmental glomerulosclerosis.

[0091] In another study, rats were given adriamycin and the effects on angiotensin converting enzyme (ACE) were monitored (Venkatesan et al. (1993) Toxicology 85: 137- 148). The rats developed glomerular and tubular injury, and serum ACE levels were significantly elevated 20,25, and 30 days post-treatment. A different study followed rabbits for up to one year that were treated with either adriamycin, nephrectomy, or combinations thereof (Gadeholt-Gothlin et al. (1995) Urol Res 23: 169-173). The rabbits that were treated with adriamycin exhibited signs of nephrotoxicity at relatively low doses.

[0092] Menadione (vitamin K3) is a fat-soluble vitamin precursor that is converted into menaquinone in the liver. The primary known function of vitamin K is to assist in normal blood clotting, but it may also play a role in bone calcificaton. Menadione is a quinone compound that induces oxidative stress. It has been used as an anticancer agent and radiosensitizer and can produce toxicity in the kidney, lung, heart, and liver. In the kidney, signs of toxicity are dose-dependent, ranging from minor degranulation of tubular cells at lower doses to tubular dilatation, formation of protein casts in the renal tubules, calcium mineralization, vacuolization in the proximal and distal renal tubules, granular degeneration in the cortex and necrosis and apoptosis (Chiou et al., Toxicology (1997) 124 (3): 193-202).

[0093] Monocrotaline, an alkaloid obtained from Crotalaria spectabilis, a warm-climate garden plant, induces multi-organ toxicity affecting the kidney, heart, liver and lung. This compound is used to induce mesangiolysis in the kidney, to mimic the effects of Habu venom poisoning and hemolytic-uremic syndrome. Renal lesions in rats first appeared in the glomerular capillaries (endothelial cell detachment and adhesion of platelets to the basal lamina), followed by severe edema in the mesangium. Mesangiolysis subsequently occurred, accompanied by dilatation or obliteration of capillaries and necrosis and hemorrhage in the mesangium (Kurozumi et al., Exp Mol Pathol (1983) 39 (3): 377-386).

[0094] Vancomycin is a polycyclic glycoprotein antibiotic that is used to treat severe systemic infections by beta-lactam-resistant bacteria, in particular, resistant staphylococci.

This drug may be given to patients who are allergic to penicillin. Vancomycin can induce renal failure and interstitial nephritis (Physicians Desk Reference 56th Ed., pp. 1970-1971, Medical Economics Co. , Montvale, New Jersey, 2002).

[0095] Sodium chromate, a model compound used to induce liver toxicity, also produces toxic effects in the kidney. Necrosis of the S 1 segment of the proximal tubule has been reported, as well as acute renal failure, characterized by increased levels of kininogens in the renal cortex and medulla and in urine and decreased rates of glomerular filtration (Bompart et al., Nephron (1993) 65 (4): 612-618; Beckwith-Hall et al., Chem Res Toxicol (1998) 11 (4): 260-272).

[0096] In the kidney, sodium oxalate forms crystals in the urinary tract, resulting in tubular obstruction, and produces calcific kidney stones in humans and in rats. The stones are located on renal papillary surfaces and consist of an organic matrix and crystals of calcium oxalate and/or calcium phosphate. The matrix is intimately associated with the crystals and contains substances that both promote and inhibit calcification: osteopontin, Tamm- Horsfall protein, bikunin and prothrombin fragment 1. Rats with these stones show decreased urine levels of magnesium and citrate, and the same is believed to occur in humans. Males of both species tend to develop calcium oxalate kidney stones, whereas females tend to form calcium phosphate stones (Khan, World J Urol (1997) 15 (4): 236-243).

[0097) Hexachloro-1,2-butadiene (HCBD) is a solvent that forms toxic conjugates and metabolites with glutathione, cysteine and N-acetyl cysteine. These then cause damage to the S 1, S2 and S3 (pars recta) segments of the proximal tubules in the outer medulla of the kidney. Mitochondrial swelling has been observed in the S 1 and S2 segments, although most of the pathological changes occur in the S2 and S3 segments (loss of brush boarder and cellular necrosis in S2, necrosis in S3). In rats, HCBD is about four times more toxic to females than to males (Ishmael et al., Toxicol Pathol (1986) 14 (2): 258-262; Ishmael et al., J Pathol (1982) 138 (2): 99-113).

[0098] Chloroform (CHC13) is widely used in the manufacture of drugs, cosmetics, plastics and cleaning agents and is a contaminant by-product in chlorinated drinking water.

Chloroform was also an early anesthetic used in humans, and, therefore, much is known regarding its toxicity. Exposure can induce liver and kidney damage and cardiac arrthymias.

[0099] Toxic levels of exposure in rodents are carcinogenic due to the chronic cycle of cell injury and repair that is induced, rather than because of direct genotoxic action. The injury to the liver and kidney are thought to occur by two different mechanisms related to its metabolism in the target organ. Studies have shown that the extent of liver and kidney damage and necrosis relates multiple factors including sex, strain, route of exposure and the vehicle used. In the kidney, biotransformation of chloroform by cytochrome P450 produces reactive intermediates, which damage mainly the renal proximal tubules. Typical signs of nephrotoxicity include proteinuria, glucosuria and increased BUN levels (Casarett & Doull's Toxicology : The Basic Science of Poisons 6th Ed., Klaasen, ed., Chap. 14, pp. 503-508, McGraw-Hill, New York, 2001 ; Smith et al., Toxicol Appl Pharmacol 70: 467-479,1983).

[00100] Diclofenac, a non-steroidal anti-inflammatory drug, is commonly administered to patients suffering from rheumatoid arthritis, osteoarthritis, and ankylosing spondylitis.

Following oral administration, diclofenac is rapidly absorbed and then metabolized in the liver by cytochrome P450 isozyme of the CYC2C subfamily (Goodman & Gilman's The Pharmacological Basis of Therapeutics 9th Ed., Hardman et al., eds. , p. 637, McGraw Hill, New York, 1996). In addition, diclofenac is used topically to treat pain due to corneal damage (Jayamanne et al., Eye ll (Pt. 1): 79-83,1997 ; Dornic et al., Am J. Ophthalmol 125 (5): 719-721,1998).

[00101] Metabolism of diclofenac in kidney tissue produces reactive oxygen species that can cause severe oxidative stress and genomic DNA fragmentation. Examination of diverse types of kidney cells for nuclei with apoptotic characteristics showed that such nuclei are found in the linings of the renal proximal and distal tubules. Additional toxic effects include elevated levels of BUN, malondialdehyde (MDA), SOD, and activated Ca+-Mg'+- endonuclease (Hickey et al., Free Radic Biol Med (2001) 31 (2): 139-152).

[00102] Thioacetamide's only significant commercial use is as a replacement for hydrogen sulfide in qualitative analyses (IARC, Vol. 7,1974). It has also been used as an organic solvent in the leather, textile and paper industries, as an accelerator in the vulcanization of buna rubber, and as a stabilizer of motor fuel. The primary routes of human exposure are inhalation and skin contact with products in which thioacetamide was used as a solvent (9th Report on Carcinogens, U. S. Dept. of Health and Human Services, Public Health Service, National Toxicology Program, http://ehp. niehs. nih. gov/roc/toc9. html).

[00103] In exposed'rats, thioacetamide was shown to accumulate in the liver and kidney, resulting in elevated levels of serum total bilirubin, aspartate aminotransferase, alanine aminotransferase, BUN, creatinine and TNFa. Impaired clearance of the toxin and increased secretion of TNFa are related to the progression of toxic effects in the liver and kidney (Nakatani et al., Liver (2001) 21 (1) : 64-70). Additional histological changes in kidney tissue include glomerular tuft collapse and interstitial haemorrhage (Caballero et al., Gut (2001) 48 (1) : 34-40).

[00104] Amphotericin B is widely used for severe life-threatening fungal infections. Its use is limited by a dose-dependent nephrotoxicity manifested by a reduction in glomerular filtration rate and tubular dysfunction. Elevated creatinine levels associated with amphotericin B are not only a marker for renal dysfunction but are also linked to the use of hemodialysis and a higher mortality rates. Therefore amphotericin B nephrotoxicity is not a benign complication and its prevention is essential (Deray et al. (2002), Nephrologie 23 (3): 119-122).

[00105] Carbon tetrachloride is a common organic solvent largely employed to make chlorofluorocarbon propellants and refrigerants, though this use has been declining steadily.

Other uses include: as dry cleaning agent and fire extinguisher, in making nylon, as a solvent for rubber cement, soaps, and insecticides. In a study in rats, carbon tetrachloride has been shown to produce nephrotoxicity. Significant increases in kidney superoxide dismutase and catalase activities and a significant decrease in glutathione peroxidase activity, as well as glomerular and tubular alterations in the renal cortex, have been observed in carbon tetrachloride-treated rats (Ozturk et al. (2003), Urology 62 (2): 353-356).

[00106] Ciprofibrate, a lipid regulating drug that decreases serum triglyceride levels and increases serum HDL cholesterol levels, along with other fibrate drugs, has been reported to induce renal dysfunction. Patients taking these drugs exhibited elevated plasma creatinine and urea levels (Broeders et al. (2000), Nephrol Dial Transplant 15 (12): 1993-1999).

[00107] Cyclosporin A is an immunosuppressant routinely given to organ transplant patients has been shown to cause kidney damage and hypertension. Its nephrotoxicity has been attributed primarily to renal haemodynamic alterations caused by afferent arteriolar vasoconstriction. Its toxic effects are also characterized by pre-glomerular disturbances and interstitial injury that may occur independently of haemodynamic changes. Given the high lipophilic activity of cyclosporin A, direct tubular injury is likely to contribute to nephrotoxicity (Carvalho da Costa et al. (2003) Nephrol Dial Transplant 18 (11): 2262- 2268).

[00108] Dantrolene, a muscle relaxant, is used to treat spasticity or muscle spasms associated with conditions such as spinal cord injuries, stroke, multiple sclerosis and cerebral palsy.

[00109] Ethylene glycol is a compound used to make antifreeze and de-icing solutions for cars, airplanes, and boats; to make polyester compounds; and as solvents in the paint and plastics industries. Ethylene glycol is also an ingredient in photographic developing solutions, hydraulic brake fluids and in inks used in stamp pads, ballpoint pens, and print shops. Ethylene glycol intoxication produces multisystem organ injury, including acute renal failure and damage to the proximal tubules, via the action of toxic metabolites, in particular glycoaldehyde and glyoxylate. These compounds caused ATP depletion, LDH degradation and release and phospholipid degradation. In addition, the low solubility of ethylene glycol metabolites causes crystal formation within the tubular lumen, contributing to a reduced glomerular filtration rate that in turn leads to renal failure (Poldeski et al.

(2001), Am JKidney Dis 38 (2): 339-348; Van Vleet et al. (2003), Semin Nephrol 23 (5): 500- 508).

[00110] Meloxicam is a non-steroidal anti-inflammatory drug (NSAID) that has hemodynamic (functional) side effects and idiosyncratic side effects on the kidney. The common link in both types of side effects seems to be renal ischemia related to prostaglandin synthesis inhibition. The key enzymes in this processes are the cyclooxygenases COX-1 and COX-2. Although COX-2 inhibition produces the antiinflammatory effect of NSAIDs, COX-1 inhibition produces gastrotoxicity (ulcers and gastrointestinal bleeding) and nephrotoxicity (Fackovcova et al. (2000), Bratisl Lek Listy 101 (8): 417-422).

[00111] Olsalazine, an anti-inflammatory drug, is used to treat ulcerative colitis (inflamed bowel). Studies in the rat have shown the kidney to be the major target organ of toxicity, where interstitial nephritis and tubular necrosis were observed. In longer term and higher dose studies, pelvic dilatation, focal mineral deposition, transitional cell hyperplasia, and congestion and/or haemorrhage and fibrosis were seen (Medsafe Data Sheets, http :// www. medsafe. govt. nz/profs/Datasheet/DSForm. asp).

[00112] Pentamidine is used in the prevention and treatment of pneumocystis carinii pneumonia (PCP). It is also used as an antiparasitic agent for the treatment of parasites.

Pentamidine is typically used when a person has experienced adverse effects or toxicity to other drugs, such as trimethoprim-sulfamethoxazole (TMP-SMX) or dapsone. Renal side- effects are frequently observed after parenteral administration of pentamidine. In studies in rats, nephrotoxicity was assessed by measuring urinary loss of tubular cells, malate dehydrogenase activity and creatinine clearance. The tubular toxicity of pentamidine appears to be dose-related and reversible (Feddersen et al. (1991) J Antimicrob Chemother 28 (3): 437-446. ) [00113] The analgesic drug phenacetin, a NSAID, was taken off the market in the United States in 1983 for causing analgesic-associated nephropathy (AAN) and subsequent end- stage renal disease. A metabolite of phenacetin is acetominophen (Tylenol@) which can also have toxic effects on the kidney. The NSAIDs exert their anti-inflammatory and fever- lowering effects by inhibiting cyclooxygenases (COX-1 and COX-2), enzymes responsible for the production of prostaglandins. Prostaglandins are not key renal blood flow mediators in healthy people with normal kidneys, but in people with a decreased blood volume or circulation problems, the kidney depends on the dilating effect on renal blood vessels of the prostaglandins to maintain renal blood flow, which is critical to maintaining renal function.

Because NSAIDs decrease prostaglandin production, people at greatest risk for renal toxicity are those who already have these problems, such as those using diuretics or those suffering from dehydration, heart failure or liver failure. Inhibition of prostaglandin synthesis by NSAIDs is also responsible for electrolyte disturbances such as increased potassium and sodium blood levels and decreased secretion of aldosterone, whose major function is to maintain blood volume when blood pressure drops. Because prostaglandins facilitate sodium excretion, some patients also may experience sodium retention when taking NSAIDs, causing edema and elevated blood pressure and exacerbating the symptoms of heart failure. People at greatest risk are those with diabetes, renal disease, circulatory complications and advanced age (Dilanchian (2002), NurseWeek, http :// www. nurseweek. com/ce/ce80a. asp).

[00114] Propyleneimine (2-methyl-aziridine) is used as an intermediate in the paper, textile, rubber, and pharmaceutical industries. It is severely irritating to the eyes and upper respiratory tract from acute (short-term) inhalation exposure in humans and is also known to cause necrosis in the renal papillae. Clinical signs of papillary toxicity are decreased urine levels of succinate and citrate elevated levels of creatine (Holmes et al. (1997) Comp BiochemPhysiol CPharmacol ToxicolEndocrinol 116 (2): 125-134).

[00115] Semustine (MeCCNU) is an anti-cancer drug has been shown to produce proximal tubule injury and papillary necrosis in rats. Progressive nephropathy, which was delayed in onset, and characterized by polyuria, enzymuria, accumulations of organic ions and decreased urine concentrating ability was observed. Administration of semustine also lead to karyomegaly in the collecting ducts in the renal medulla (Kramer et al. (1986), Toxicol Appl Pharmacol 82 (3): 540-550).

[00116] Suramin is an anti-parasitic drug and reverse transcriptase inhibitor that is used to treat metastatic cancer. This compound is known to inhibit the binding of growth factors (e. g., epidermal growth factor (EGF), platelet-derived growth factor (PDGF) and tumor growth factor-beta (TGF-beta) ) to their receptors and thus antagonize the ability of these factors to stimulate growth of tumor cells in vitro. Experiments in rats have shown that the renal parenchyma is adversely affected by exposure to the drug. Marked and widespread alterations were detected in both cortex and medulla, indicating that suramin induces severe chronic renal damage in rats (Soldani et al. (1992) In Vivo 6 (6): 617-620).

[00117] Tacrolimus is another immunosuppressant routinely given to organ transplant patients. In the kidneys, proximal tubular epithelial cells (PTEC) tend to undergo apoptosis in response to immunosuppressors such as tacrolimus and participate in the onset of several renal diseases. Immunosuppressors probably induce apoptosis through a mechanism that involves the irreversible opening of the mitochondrial permeability transition pore.

Activation of caspases 3 and 7 has also been observed. Apoptosis in the proximal tubules may contribute to the renal toxicity that is observed in the course of immunosuppressive therapy.

Toxicity Prediction and Modeling [00118] The genes and gene expression information (including Tox Group Mean, Non-tox Group Mean, LDA score and PLS score for each gene), gene expression profiles, as well as the portfolios and subsets of the genes provided in Tables 1-5N, may be used to predict at least one toxic effect, including the nephrotoxicity of a test or unknown compound. As used, herein, at least one toxic effect includes, but is not limited to, a detrimental change in the physiological status of a cell or organism. The response may be, but is not required to be, associated with a particular pathology, such as tissue necrosis. Accordingly, the toxic effect includes effects at the molecular and cellular level. Nephrotoxicity is an effect as used herein and includes but is not limited to the pathologies of nephritis, tubular toxicity, kidney necrosis, glomerular and tubular injury, and focal segmental glomerulosclerosis. As used herein, a gene expression profile comprises any quantitative representation of the expression of at least one mRNA species in a cell sample or population and includes profiles made by various methods such as differential display, PCR, microarray and other hybridization analysis, etc.

[00119] In general, assays to predict the toxicity or nephrotoxicity of a test agent (or compound or multi-component composition) comprise the steps of exposing a cell population to the test compound, assaying or measuring the level of relative or absolute gene expression of one or more of the genes in Tables 1-5N and comparing the identified expression level (s) to the expression levels or other representations of expression levels disclosed in the Tables and database (s) disclosed herein. Such gene expression information includes the Tox Group Mean, Non-tox Group Mean, LDA (linear discriminant analysis) score and PLS (partial least squares) score for the genes listed in Tables 5A-5N. Assays may include the measurement of the expression levels of about 2,3, 4,5, 6,7, 8,9, 10,15, 20,25, 30,50, 75,100, 200,500, 1000 or more genes from Tables 1-5N, or ranges of these numbers, such as about 2-10, about 10-20, about 20-50, about 50-100, about 100-200, about 200-500 or about 500-1000 genes from Tables 1-5N. Assays for toxicity prediction may also include the measurement of nearly all the genes in Tables 1-5N."Nearly all"the genes may be considered to mean at least 80% of the genes in any one of or all of Tables 1-5N.

[00120] In some methods of the invention, the gene expression level for a gene or genes induced by the test agent, compound or compositions may be comparable to the levels found in the Tables or databases disclosed herein if the expression level varies within a factor of about 2, about 1.5 or about 1.0 fold. In some cases, the expression levels are comparable if the agent induces a change in the expression of a gene in the same direction (e. g., up or down) as a reference toxin.

[00121] In other methods of the invention, an RMA (robust multi-array average) fold- change value for the gene or genes of a gene expression profile using data from a test compound-exposed sample and from a control vehicle-exposed sample is calculated (see Irizarry et al. (2003), "Summaries of Affymetrix GeneChip probe level data,"Nucl Acids Res 31 (4): el5, 8 pp.; and Irizarry et al. (2003), "Exploration, normalization, and summaries of high density oligonucleotide array probe level data,"Biostatistics 4 (2): 249-264, both of which are incorporated herein by reference in their entirety). The RMA fold-change value may then be multiplied on a gene-by-gene basis by a PLS weight (or PLS score, see Table 5N) for each gene and these resulting values can be summed across all the genes or across a selected set of genes. This sum creates a single predictive score for the sample.

Comparison of this predictive score with a cut-off value, as provided herein, indicates whether or not the test compound has induced at least one toxic response.

[00122] The cell population that is exposed to the test agent, compound or composition may be exposed in vitro or in vivo. For instance, cultured or freshly isolated renal cells, in particular rat renal cells, may be exposed to the agent under standard laboratory and cell culture conditions. In another assay format, in vivo exposure may be accomplished by administration of the agent to a living animal, for instance a laboratory rat.

[00123] Procedures for designing and conducting toxicity tests in in vitro and in vivo systems are well known, and are described in many texts on the subject, such as Loomis et al., Loomis's Esstentials of Toxicology, 4th Ed. , Academic Press, New York, 1996; Echobichon, The Basics of Toxicity Testing, CRC Press, Boca Raton, 1992; Frazier, editor, In Vitro Toxicity Testing, Marcel Dekker, New York, 1992; and the like.

[00124] In in vitro toxicity testing, two groups of test organisms are usually employed: One group serves as a control and the other group receives the test compound in a single dose (for acute toxicity tests) or a regimen of doses (for prolonged or chronic toxicity tests).

Because, in some cases, the extraction of tissue as called for in the methods of the invention requires sacrificing the test animal, both the control group and the group receiving compound must be large enough to permit removal of animals for sampling tissues, if it is desired to observe the dynamics of gene expression through the duration of an experiment.

[00125] In setting up a toxicity study, extensive guidance is provided in the literature for selecting the appropriate test organism for the compound being tested, route of administration. dose ranges, and the like. Water or physiological saline (0.9% NaCI in water) is the solute of choice for the test compound since these solvents permit administration by a variety of routes. When this is not possible because of solubility limitations, vegetable oils such as corn oil or organic solvents such as propylene glycol may be used.

[00126] Regardless of the route of administration, the volume required to administer a given dose is limited by the size of the animal that is used. It is desirable to keep the volume of each dose uniform within and between groups of animals. When rats or mice are used, the volume administered by the oral route generally should not exceed about 0.005 ml per gram of animal. Even when aqueous or physiological saline solutions are used for parenteral injection the volumes that are tolerated are limited, although such solutions are ordinarily thought of as being innocuous. The intravenous LD50 of distilled water in the mouse is approximately 0.044 ml per gram and that of isotonic saline is 0.068 ml per gram of mouse. In some instances, the route of administration to the test animal should be the same as, or as similar as possible to, the route of administration of the compound to man for therapeutic purposes.

[00127] When a compound is to be administered by inhalation, special techniques for generating test atmospheres are necessary. The methods usually involve aerosolization or nebulization of fluids containing the compound. If the agent to be tested is a fluid that has an appreciable vapor pressure, it may be administered by passing air through the solution under controlled temperature conditions. Under these conditions, dose is estimated from the volume of air inhaled per unit time, the temperature of the solution, and the vapor pressure of the agent involved. Gases are metered from reservoirs. When particles of a solution are to be administered, unless the particle size is less than about 2 um the particles will not reach the terminal alveolar sacs in the lungs. A variety of apparatuses and chambers are available to perform studies for detecting effects of irritant or other toxic endpoints when they are administered by inhalation. The preferred method of administering an agent to animals is via the oral route, either by intubation or by incorporating the agent in the feed.

[00128] When the agent is exposed to cells in vitro or in cell culture, the cell population to be exposed to the agent may be divided into two or more subpopulations, for instance, by dividing the population into two or more identical aliquots. In some preferred embodiments of the methods of the invention, the cells to be exposed to the agent are derived from kidney tissue. For instance, cultured or freshly isolated rat renal cells may be used.

[00129] The methods of the invention may be used generally to predict at least one toxic response, and, as described in the Examples, may be used to predict the likelihood that a compound or test agent will induce various specific kidney pathologies, such as nephritis, kidney necrosis, glomerular and tubular injury, focal segmental glomerulosclerosis, or other pathologies associated with at least one of the toxins herein described. The methods of the invention may also be used to determine the similarity of a toxic response to one or more individual compounds. In addition, the methods of the invention may be used to predict or elucidate the potential cellular pathways influenced, induced or modulated by the compound or test agent due to the similarity of the expression profile compared to the profile induced by a known toxin (see Tables 1-5N). In particular, Table 2 provides a description of metabolic pathways in which each listed gene is involved.

Building a Database for Toxicity Prediction-RMA/PLS [00130] In the present invention, a toxicity study or"tox study"comprises a set of cell or tissue samples from rats. These samples are organized into cohorts by test compound, time (time from initial test compound dosage at which the rats were sacrificed), and dose (amount of test compound administered). All cohorts in a tox study share the same vehicle control. For example, a cohort may be a set of samples from rats that were treated with acyclovir for 6 hours at a high dosage (100 mg/kg). A time-matched vehicle cohort is a set of samples that serve as controls for treated animals within a tox study, e. g., for 6-hour acyclovir-treated high dose samples the time-matched vehicle cohort would be the 6-hour vehicle-treated samples with that study.

[00131] A toxicity database or"tox database"is a set of tox studies that comprises a reference database. The reference database includes data from rat tissue and cell samples from rats that were treated with different test compounds at different dosages and exposed to the test compounds for varying lengths of time. RMA, or robust multi-array average, is an algorithm that converts raw fluorescence intensities, such as those derived from hybridization of sample nucleic acids to an Affymetrix GeneChipt), into expression values, one value for each gene fragment on a chip (Irizarry et al. (2003), Nucleic Acids Res.

31 (4): el5, 8 pp. ). RMA produces values on a log2 scale, typically between 4 and 12 for genes that are expressed significantly above or below control levels. These RMA values can be positive or negative and are centered around zero for a fold-change of about 1. PLS, or Partial Least Squares, is a modeling algorithm that takes as inputs a matrix of predictors and a vector of supervised scores to generate a set of prediction weights for each of the input predictors (Nguyen et al. (2002), Bioinformatics 18: 39-50). These prediction weights can be converted to PLS scores to indicate the ability of each analyzed gene to predict a toxic response. RMA generates a matrix of gene expression values that can be subjected to PLS to produce a model for prediction of toxic responses, e. g. , a model for predicting kidney toxicity.

[00132] Although other algorithms for analyzing DNA microarrays are known the art, present inventors have found that the combination of RMA and PLS provides greater accuracy in sample measurements and improved ability to use external data (data from tox studies that have not been added to a tox database). In RMA/PLS models, it was found that external data sets that may be viewed as incompatible according to other algorithms have little impact on the ability of the model to predict a toxic response if these data sets are added to the model. Consequently, an external data set may not require an assessment of compatibility. Additionally, this model allows all sample time points to be used, as all time points for high-dose toxin-treated samples are compared to all time points for non-toxin- treated samples, negative controls, vehicle control and low-dose-treated samples. Further, the model is not affected by the distribution of genes in a sample, and the rates of true positive samples are increased. Using these algorithms, evaluation of the similarity of test compounds is also improved, because a model containing a correlation matrix is generated, rather than separate models for each test compound.

Building a Database for Toxicity Prediction-MAS/LDA [00133] In some embodiments of the present invention, a database for predicting kidney toxicity may be built from gene expression information from DNA microarrays that was generated by using the Affymetrixe MAS4 or MAS5 algorithms. These gene expression values are derived from fluorescence intensity measurements of probe pairs, a perfect match (PM) and a mismatch (MM), after hybridization to a target sequence. The data are converted to a log2 scale and are corrected for background and normalized (see Irizarry et al., Nucl Acids Res, supra). Linear discriminant analysis (LDA) methods may then be applied to identify the genes in a gene expression profile that have the best ability to predict a toxic response. LDA is a classical statistical approach for classifying samples of unknown classes, based on training samples with known classes. LDA has been previously applied to sample classification of microarray data (Hakak et al. (2001), Proc Natl Acad Sci USA 98 (8): 4746-4751 ; Dudoit et al. (2002), JAm Statistical Association, 97 (457): 77-87) and can be used to identify genes that are differentially expressed (up-or down-regulated) in pairwise comparisons. LDA seeks the linear combination of variables that maximizes the ratio of between-group variance and within-group variance by using grouping information.

For two groups, the linear weights in LDA depend on how a gene separates in the two groups and how a gene correlates with other genes.

Diagnostic Usesfor the Toxicity Markers [00134] As described above, the genes and gene expression information or portfolios of the genes with their expression information as provided in Tables 1-5N may be used as diagnostic markers for the prediction or identification of the physiological state of tissue or cell sample that has been exposed to a compound or to identify or predict the toxic effects of a compound or agent. For instance, a tissue sample, such as kidney tissue, or a sample of peripheral blood cells or some other easily obtainable tissue, may be assayed by any of the methods described above, and the expression levels from a gene or genes from Tables 1-5N may be compared to the expression levels or related data found in tissues or cells exposed to the toxins described herein. These methods may result in the diagnosis of a physiological state in the cell or may be used to identify the potential toxicity of a compound, for instance a new or unknown compound or agent. The comparison of expression data, as well as available sequence or other information may be done by researcher or diagnostician or may be done with the aid of a computer and databases as described below.

[00135] In another format, the levels of a gene (s) of Tables 1-5N, its encoded protein (s), or any metabolite produced by the encoded protein may be monitored or detected in a sample, such as a bodily tissue or fluid sample to identify or diagnose a physiological state of an organism. Such samples may include any tissue or fluid sample, including urine, blood and easily obtainable cells such as peripheral lymphocytes.

Use of the Markers for Monitoring Toxicity Progression [00136] As described above, the genes and gene expression information provided in Tables 1-5N may also be used as markers for the monitoring of toxicity progression, such as that found after initial exposure to a drug, drug candidate, toxin, pollutant, etc. For instance, a tissue or cell sample may be assayed by any of the methods described above, and the expression levels from a gene or genes from Tables 1-5N may be compared to the expression levels or related data found in tissue or cells exposed to the renal toxins described herein. The comparison of the expression data, as well as available sequence or other information may be done by a researcher or diagnostician or may be done with the aid of a computer and databases.

Use of the Toxicity Markers for Drug Screening [00137] According to the present invention, the genes identified in Tables 1-5N may be used as markers or drug targets to evaluate the effects of a candidate drug, chemical compound or other agent on a cell or tissue sample. The genes may also be used as drug targets to screen for agents that modulate their expression and/or activity. In various formats, a candidate drug or agent can be screened for the ability to stimulate the transcription or expression of a given marker or markers or to down-regulate or counteract the transcription or expression of a marker or markers. According to the present invention, one can also compare the specificity of a drug's effects by looking at the number of markers which the drug induces and comparing them. More specific drugs will have less transcriptional targets. Similar sets of markers identified for two drugs may indicate a similarity of effects.

[00138] Assays to monitor the expression of a marker or markers as defined in Tables 1-5N may utilize any available means of monitoring for changes in the expression level of the nucleic acids of the invention. As used herein, an agent is said to modulate the expression of a nucleic acid of the invention if it is capable of up-or down-regulating expression of the nucleic acid in a cell.

[00139] In one assay format, gene chips containing probes to one, two or more genes from Tables 1-5N may be used to directly monitor or detect changes in gene expression in the treated or exposed cell. Cell lines, tissues or other samples are first exposed to a test agent and in some instances, a known toxin, and the detected expression levels of one or more, or preferably 2 or more of the genes of Tables 1-5N are compared to the expression levels or related data of those same genes exposed to a known toxin alone. Compounds that modulate the expression patterns of the known toxin (s) would be expected to modulate potential toxic physiological effects in vivo. The genes in Tables 1-5N are particularly appropriate markers in these assays as they are differentially expressed in cells upon exposure to a known renal toxin. Table 1 discloses those genes that are differentially expressed upon exposure to the named toxins and their corresponding GenBank Accession numbers and Unigene cluster titles. Table 2 indicates the metabolic pathways in which some of the genes in Table 1 function. Table 3 discloses the human homologues of some of the differentially expressed genes in Tables 1 and 2.

[00140] In another format, cell lines that contain reporter gene fusions between the open reading frame and/or the transcriptional regulatory regions of a gene in Tables 1-5N and any assayable fusion partner may be prepared. Numerous assayable fusion partners are known and readily available including the firefly luciferase gene and the gene encoding chloramphenicol acetyltransferase (Alam et al. (1990), Anal Biochem 188: 245-254). Cell lines containing the reporter gene fusions are then exposed to the agent to be tested under appropriate conditions and time. Differential expression of the reporter gene between samples exposed to the agent and control samples identifies agents which modulate the expression of the nucleic acid.

[00141] Additional assay formats may be used to monitor the ability of the agent to modulate the expression of a gene identified in Tables 1-5N. For instance, as described above, mRNA expression may be monitored directly by hybridization of probes to the nucleic acids of the invention. Cell lines are exposed to the agent to be tested under appropriate conditions and time, and total RNA or mRNA is isolated by standard procedures such those disclosed in Sambrook et al. (Molecular Cloning: A Laboratory Manual, 2nd Ex.., Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY, 1989).

[00142] In another assay format, cells or cell lines are first identified which express the gene products of the invention physiologically. Cells and/or cell lines so identified would be expected to comprise the necessary cellular machinery such that the fidelity of modulation of the transcriptional apparatus is maintained with regard to exogenous contact of agent with appropriate surface transduction mechanisms and/or the cytosolic cascades.

Further, such cells or cell lines may be transduced or transfected with an expression vehicle (e. g., a plasmid or viral vector) construct comprising an operable non-translated 5'-promoter containing end of the structural gene encoding the gene products of Tables 1-5N fused to one or more antigenic fragments or other detectable markers, which are peculiar to the instant gene products, wherein said fragments are under the transcriptional control of said promoter and are expressed as polypeptides whose molecular weight can be distinguished from the naturally occurring polypeptides or may further comprise an immunologically distinct or other detectable tag. Such a process is well known in the art (see Sambrook et al., supra).

[00143] Cells or cell lines transduced or transfected as outlined above are then contacted with agents under appropriate conditions; for example, the agent comprises a pharmaceutically acceptable excipient and is contacted with cells comprised in an aqueous physiological buffer such as phosphate buffered saline (PBS) at physiological pH, Eagles balanced salt solution (BSS) at physiological pH, PBS or BSS comprising serum or conditioned media comprising PBS or BSS and/or serum incubated at 37°C. Said conditions may be modulated as deemed necessary by one of skill in the art. Subsequent to contacting the cells with the agent, said cells are disrupted and the polypeptides of the lysate are fractionated such that a polypeptide fraction is pooled and contacted with an antibody to be further processed by immunological assay (e. g., ELISA, immunoprecipitation or Western blot). The pool of proteins isolated from the agent-contacted sample is then compared with the control samples (no exposure and exposure to a known toxin) where only the excipient is contacted with the cells and an increase or decrease in the immunologically generated signal from the agent-contacted sample compared to the control is used to distinguish the effectiveness and/or toxic effects of the agent.

[00144] Another embodiment of the present invention provides methods for identifying agents that modulate at least one activity of a protein (s) encoded by the genes in Tables 1- 5N. Such methods or assays may utilize any means of monitoring or detecting the desired activity.

[00145] In one format, the relative amounts of a protein (Tables 1-5N) between a cell population that has been exposed to the agent to be tested compared to an un-exposed control cell population and a cell population exposed to a known toxin may be assayed. In this format, probes such as specific antibodies are used to monitor the differential expression of the protein in the different cell populations. Cell lines or populations are exposed to the agent to be tested under appropriate conditions and time. Cellular lysates may be prepared from the exposed cell line or population and a control, unexposed cell line or population. The cellular lysates are then analyzed with the probe, such as a specific antibody.

[00146] Agents that are assayed in the above methods can be randomly selected or rationally selected or designed. As used herein, an agent is said to be randomly selected when the agent is chosen randomly without considering the specific sequences involved in the association of a protein of the invention alone or with its associated substrates, binding partners, etc. An example of randomly selected agents is the use a chemical library or a peptide combinatorial library, or a growth broth of an organism.

[00147] As used herein, an agent is said to be rationally selected or designed when the agent is chosen on a nonrandom basis which takes into account the sequence of the target site and/or its conformation in connection with the agent's action. Agents can be rationally selected or rationally designed by utilizing the peptide sequences that make up these sites.

For example, a rationally selected peptide agent can be a peptide whose amino acid sequence is identical to or a derivative of any functional consensus site.

[00148] The agents of the present invention can be, as examples, peptides, small molecules, vitamin derivatives, as well as carbohydrates. Dominant negative proteins, DNAs encoding these proteins, antibodies to these proteins, peptide fragments of these proteins or mimics of these proteins may be introduced into cells to affect function. "Mimic"used herein refers to the modification of a region or several regions of a peptide molecule to provide a structure chemically different from the parent peptide but topographically and functionally similar to the parent peptide (see G. A. Grant in: Molecular Biology and Biotechnology, Meyers, ed., pp. 659-664, VCH Publishers, New York, 1995). A skilled artisan can readily recognize that there is no limit as to the structural nature of the agents of the present invention.

Nucleic Acid Assay Formats [00149] The genes identified as being differentially expressed upon exposure to a known renal toxin (Tables 1-5N) may be used in a variety of nucleic acid detection assays to detect or quantify the expression level of a gene or multiple genes in a given sample. The genes described in Tables 1-5N may also be used in combination with one or more additional genes whose differential expression is associate with toxicity in a cell or tissue. In preferred embodiments, the genes in Tables 1-5N may be combined with one or more of the genes described in prior and related applications 10/301,856, filed November 22,2002 ; 10/152,319, filed May 22,2002 ; 60/292,335, filed May 22,2001 ; 60/297,523, filed June 13, 2001; 60/298,925, filed June 19,2001 ; 60/303,810, filed July 10,2001 ; 60/303,807, filed July 10,2001 ; 60/303,808, filed July 10,2001 ; 60/315,047, filed August 28,2001 ; 60/324,928, filed September 27,2001 ; 60/330,867, filed November 1, 2001; 60/330,462, filed October 22,2001 ; 60/331,805, filed November 21,2001 ; 60/336,144, filed December 6,2001 ; 60/340,873, filed December 19,2001 ; 60/357,843, filed February 21,2002 ; 60/357,842, filed February 21,2002 ; 60/357,844, filed February 21,2002 ; 60/364,134 ; 60/370,206 filed March 15,2002, filed April 8,2002 ; 60/370,247, filed April 8,2002 ; 60/370,144, filed April 8,2002 ; 60/371, 679, filed April 12,2002 ; and 60/372, 794, filed April 17,2002, all of which are incorporated by reference on page 1 of this application.

[00150] Any assay format to detect gene expression may be used. For example, traditional Northern blotting, dot or slot blot, nuclease protection, primer directed amplification, RT- PCR, semi-or quantitative PCR, branched-chain DNA and differential display methods may be used for detecting gene expression levels. Those methods are useful for some embodiments of the invention. In cases where smaller numbers of genes are detected, amplification based assays may be most efficient. Methods and assays of the invention, however, may be most efficiently designed with hybridization-based methods for detecting the expression of a large number of genes.

[00151] Any hybridization assay format may be used, including solution-based and solid support-based assay formats. Solid supports containing oligonucleotide probes for differentially expressed genes of the invention can be filters, polyvinyl chloride dishes, particles, beads, microparticles or silicon or glass based chips, etc. Such chips, wafers and hybridization methods are widely available, for example, those disclosed by Beattie (WO 95/11755).

[00152] Any solid surface to which oligonucleotides can be bound, either directly or indirectly, either covalently or non-covalently, can be used. A preferred solid support is a high density array or DNA chip. These contain a particular oligonucleotide probe in a predetermined location on the array. Each predetermined location may contain more than one molecule of the probe, but each molecule within the predetermined location has an identical sequence. Such predetermined locations are termed features. There may be, for example, from 2,10, 100,1000 to 10,000, 100,000 or 400,000 or more of such features on a single solid support. The solid support, or the area within which the probes are attached may be on the order of about a square centimeter. Probes corresponding to the genes of Tables 1-5N or from the related applications described above may be attached to single or multiple solid support structures, e. g. , the probes may be attached to a single chip or to multiple chips to comprise a chip set.

[00153] Oligonucleotide probe arrays for expression monitoring can be made and used according to any techniques known in the art (see for example, Lockhart et al. (1996), Nat Biotechnol 14 : 1675-1680; McGall et al. (1996), Proc Nat Acad Sci USA 93: 13555-13460).

Such probe arrays may contain at least two or more oligonucleotides that are complementary to or hybridize to two or more of the genes described in Tables 1-5N. For instance, such arrays may contain oligonucleotides that are complementary to or hybridize to at least 2,3, 4, 5, 6,7, 8,9, 10,20, 30,50, 70,100 or more of the genes described herein.

Preferred arrays contain all or nearly all of the genes listed in Tables 1-SN, or individually, the gene sets of Tables 5A-5N. In a preferred embodiment, arrays are constructed that contain oligonucleotides to detect all or nearly all of the genes in any one of or all of Tables 1-5N on a single solid support substrate, such as a chip.

[00154] The sequences of the expression marker genes of Tables 1-5N are in the public databases. Table 1 provides the GenBank Accession Number or NCBI RefSeq ID for each of the sequences (see www. ncbi. nlm. nih. gov/), as well as the title for the cluster of which gene is part. Table 2 lists the metabolic pathways in which each listed gene functions, while Table 3 provides the gene names and cluster titles for the human homologues of the genes described in Tables 1 and 2. The sequences of the genes in GenBank and/or RefSeq are expressly herein incorporated by reference in their entirety as of the filing date of this application, as are related sequences, for instance, sequences from the same gene of different lengths, variant sequences, polymorphic sequences, genomic sequences of the genes and related sequences from different species, including the human counterparts, where appropriate. These sequences may be used in the methods of the invention or may be used to produce the probes and arrays of the invention. In some embodiments, the genes in Tables 1-SN that correspond to the genes or fragments previously associated with a toxic response may be excluded from the Tables. Table 4 provides the key to the model codes used in Tables 3 and 5A-5L, where each model represents a toxin treatment or a set of pathological effects (disease state) resulting from a toxin treatment. In Tables 5A-5N, the genes that are differentially expressed, i. e. , up-or down-regulated, in response to a toxin treatment or in a particular disease state are listed. The expression levels of these genes in samples in which a toxic response was found and in samples in which a toxic response was not found are also indicated.

[00155] As described above, in addition to the sequences of the GenBank Accession Numbers or NCBI RefSeq ID's disclosed in the Tables 1-5N, sequences such as naturally occurring variants or polymorphic sequences may be used in the methods and compositions of the invention. For instance, expression levels of various allelic or homologous forms of a gene disclosed in Tables 1-5N may be assayed, including homologs from species other than rat. Any and all nucleotide variations that do not alter the functional activity of a gene listed in the Tables 1-5N, including all naturally occurring allelic variants of the genes herein disclosed, may be used in the methods and to make the compositions (e. g. , arrays) of the invention.

[00156] Probes based on the sequences of the genes described above may be prepared by any commonly available method. Oligonucleotide probes for screening or assaying a tissue or cell sample are preferably of sufficient length to specifically hybridize only to appropriate, complementary genes or transcripts. Typically the oligonucleotide probes will be at least about 10,12, 14,16, 18,20 or 25 nucleotides in length. In some cases, longer probes of at least about 30,40, or 50 nucleotides will be desirable.

[00157] As used herein, oligonucleotide sequences that are complementary to one or more of the genes described in Tables 1-5N refer to oligonucleotides that are capable of hybridizing under stringent conditions to at least part of the nucleotide sequences of said genes. Such hybridizable oligonucleotides will typically exhibit at least about 75% sequence identity at the nucleotide level to said genes, preferably about 80% or 85% sequence identity or more preferably about 90% or 95% or more sequence identity to said genes.

[00158]"Bind (s) substantially"refers to complementary hybridization between a probe nucleic acid and a target nucleic acid and embraces minor mismatches that can be accommodated by reducing the stringency of the hybridization media to achieve the desired detection of the target polynucleotide sequence.

[00159] The terms"background"or"background signal intensity"refer to hybridization signals resulting from non-specific binding, or other interactions, between the labeled target nucleic acids and components of the oligonucleotide array (e. g. , the oligonucleotide probes, control probes, the array substrate, etc.). Background signals may also be produced by intrinsic fluorescence of the array components themselves. A single background signal can be calculated for the entire array, or a different background signal may be calculated for each target nucleic acid. In a preferred embodiment, background is calculated as the average hybridization signal intensity for the lowest 5% to 10% of the probes in the array, or, where a different background signal is calculated for each target gene, for the lowest 5% to 10% of the probes for each gene. Of course, one of skill in the art will appreciate that where the probes to a particular gene hybridize well and thus appear to be specifically binding to a target sequence, they should not be used in a background signal calculation.

Alternatively, background may be calculated as the average hybridization signal intensity produced by hybridization to probes that are not complementary to any sequence found in the sample (e. g. probes directed to nucleic acids of the opposite sense or to genes not found in the sample such as bacterial genes where the sample is mammalian nucleic acids).

Background can also be calculated as the average signal intensity produced by regions of the array that lack any probes at all.

[00160] The phrase"hybridizing specifically to"or"specifically hybridizes"refers to the binding, duplexing, or hybridizing of a molecule substantially to or only to a particular nucleotide sequence or sequences under stringent conditions when that sequence is present in a complex mixture (e. g. , total cellular) DNA or RNA.

[00161] Assays and methods of the invention may utilize available formats to simultaneously screen at least about 100, preferably about 1000, more preferably about 10,000 and most preferably about 1,000, 000 different nucleic acid hybridizations.

[00162] As used herein a"probe"is defined as a nucleic acid, capable of binding to a target nucleic acid of complementary sequence through one or more types of chemical bonds, usually through complementary base pairing, usually through hydrogen bond formation. As used herein, a probe may include natural (i. e., A, G, U, C, or T) or modified bases (7- deazaguanosine, inosine, etc.). In addition, the bases in probes may be joined by a linkage other than a phosphodiester bond, so long as it does not interfere with hybridization. Thus, probes may be peptide nucleic acids in which the constituent bases are joined by peptide bonds rather than phosphodiester linkages.

[00163] The term"perfect match probe"refers to a probe that has a sequence that is perfectly complementary to a particular target sequence. The test probe is typically perfectly complementary to a portion (subsequence) of the target sequence. The perfect match (PM) probe can be a"test probe", a"normalization control"probe, an expression level control probe and the like. A perfect match control or perfect match probe is, however, distinguished from a"mismatch control"or"mismatch probe." [00164] The terms"mismatch control"or"mismatch probe"refer to a probe whose sequence is deliberately selected not to be perfectly complementary to a particular target sequence. For each mismatch (MM) control in a high-density array there typically exists a corresponding perfect match (PM) probe that is perfectly complementary to the same particular target sequence. The mismatch may comprise one or more bases.

[00165] While the mismatch (es) may be located anywhere in the mismatch probe, terminal mismatches are less desirable as a terminal mismatch is less likely to prevent hybridization of the target sequence. In a particularly preferred embodiment, the mismatch is located at or near the center of the probe such that the mismatch is most likely to destabilize the duplex with the target sequence under the test hybridization conditions.

[00166] The term"stringent conditions"refers to conditions under which a probe will hybridize to its target subsequence, but with only insubstantial hybridization to other sequences or to other sequences such that the difference may be identified. Stringent conditions are sequence-dependent and will be different in different circumstances. Longer sequences hybridize specifically at higher temperatures. Generally, stringent conditions are selected to be about 5°C lower than the thermal melting point (Tm) for the specific sequence at a defined ionic strength and pH.

[00167] Typically, stringent conditions will be those in which the salt concentration is at least about 0.01 to 1.0 M Na+ ion concentration (or other salts) at pH 7.0 to 8.3 and the temperature is at least about 30°C for short probes (e. g., 10 to 50 nucleotides). Stringent conditions may also be achieved with the addition of destabilizing agents such as formamide.

[00168] The"percentage of sequence identity"or"sequence identity"is determined by comparing two optimally aligned sequences or subsequences over a comparison window or span, wherein the portion of the polynucleotide sequence in the comparison window may optionally comprise additions or deletions (i. e. , gaps) as compared to the reference sequence (which does not comprise additions or deletions) for optimal alignment of the two sequences. The percentage is calculated by determining the number of positions at which the identical submit (e. g. nucleic acid base or amino acid residue) occurs in both sequences to yield the number of matched positions, dividing the number of matched positions by the total number of positions in the window of comparison and multiplying the result by 100 to yield the percentage of sequence identity. Percentage sequence identity when calculated using the programs GAP or BESTFIT (see below) is calculated using default gap weights.

Probe design [00169] One of skill in the art will appreciate that an enormous number of array designs are suitable for the practice of this invention. The high density array will typically include a number of test probes that specifically hybridize to the sequences of interest. Probes may be produced from any region of the genes identified in the Tables and the attached representative sequence listing. In instances where the gene reference in the Tables is an EST, probes may be designed from that sequence or from other regions of the corresponding full-length transcript that may be available in any of the sequence databases, such as those herein described. See WO 99/32660 for methods of producing probes for a given gene or genes. In addition, any available software may be used to produce specific probe sequences, including, for instance, software available from Molecular Biology Insights, Olympus Optical Co. and Biosoft International. In a preferred embodiment, the array will also include one or more control probes.

[00170] High density array chips of the invention include"test probes. "Test probes may be oligonucleotides that range from about 5 to about 500, or about 7 to about 50 nucleotides, more preferably from about 10 to about 40 nucleotides and most preferably from about 15 to about 35 nucleotides in length. In other particularly preferred embodiments, the probes are 20 or 25 nucleotides in length. In another preferred embodiment, test probes are double or single strand DNA sequences such as cDNA fragments. DNA sequences are isolated or cloned from natural sources or amplified from natural sources using native nucleic acid as templates. These probes have sequences complementary to particular subsequences of the genes whose expression they are designed to detect. Thus, the test probes are capable of specifically hybridizing to the target nucleic acid they are to detect.

[00171] In addition to test probes that bind the target nucleic acid (s) of interest, the high density array can contain a number of control probes. The control probes may fall into three categories referred to herein as 1) normalization controls; 2) expression level controls; and 3) mismatch controls.

[00172] Normalization controls are oligonucleotide or other nucleic acid probes that are complementary to labeled reference oligonucleotides or other nucleic acid sequences that are added to the nucleic acid sample to be screened. The signals obtained from the normalization controls after hybridization provide a control for variations in hybridization conditions, label intensity, "reading"efficiency and other factors that may cause the signal of a perfect hybridization to vary between arrays. In a preferred embodiment, signals (e. g., fluorescence intensity) read from all other probes in the array are divided by the signal (e. g., fluorescence intensity) from the control probes thereby normalizing the measurements.

[00173] Virtually any probe may serve as a normalization control. However, it is recognized that hybridization efficiency varies with base composition and probe length.

Preferred normalization probes are selected to reflect the average length of the other probes present in the array, however, they can be selected to cover a range of lengths. The normalization control (s) can also be selected to reflect the (average) base composition of the other probes in the array, however in a preferred embodiment, only one or a few probes are used and they are selected such that they hybridize well (i. e. , no secondary structure) and do not match any target-specific probes.

[00174] Expression level controls are probes that hybridize specifically with constitutively expressed genes in the biological sample. Virtually any constitutively expressed gene provides a suitable target for expression level controls. Typically expression level control probes have sequences complementary to subsequences of constitutively expressed "housekeeping genes"including, but not limited to the actin gene, the transferrin receptor gene, the GAPDH gene, and the like.

[00175] Mismatch controls may also be provided for the probes to the target genes, for expression level controls or for normalization controls. Mismatch controls are oligonucleotide probes or other nucleic acid probes identical to their corresponding test or control probes except for the presence of one or more mismatched bases. A mismatched base is a base selected so that it is not complementary to the corresponding base in the target sequence to which the probe would otherwise specifically hybridize. One or more mismatches are selected such that under appropriate hybridization conditions (e. g., stringent conditions) the test or control probe would be expected to hybridize with its target sequence, but the mismatch probe would not hybridize (or would hybridize to a significantly lesser extent). Preferred mismatch probes contain a central mismatch. Thus, for example, where a probe is a 20 mer, a corresponding mismatch probe will have the identical sequence except for a single base mismatch (e. g., substituting a G, a C or a T for an A) at any of positions 6 through 14 (the central mismatch).

[00176] Mismatch probes thus provide a control for non-specific binding or cross hybridization to a nucleic acid in the sample other than the target to which the probe is directed. For example, if the target is present the perfect match probes should be consistently brighter than the mismatch probes. In addition, if all central mismatches are present, the mismatch probes can be used to detect a mutation, for instance, a mutation of a gene in the accompanying Tables 1-5N. The difference in intensity between the perfect match and the mismatch probe provides a good measure of the concentration of the hybridized material.

Nucleic Acid Samples [00177] Cell or tissue samples may be exposed to the test agent in vitro or in vivo. When cultured cells or tissues are used, appropriate mammalian cell extracts, such as liver extracts, may also be added with the test agent to evaluate agents that may require biotransformation to exhibit toxicity. In a preferred format, primary isolates or cultured cell lines of animal or human renal cells may be used.

[00178] The genes which are assayed according to the present invention are typically in the form of mRNA or reverse transcribed mRNA. The genes may or may not be cloned. The genes may or may not be amplified. The cloning and/or amplification do not appear to bias the representation of genes within a population. In some assays, it may be preferable, however, to use polyA+ RNA as a source, as it can be used with less processing steps.

[00179] As is apparent to one of ordinary skill in the art, nucleic acid samples used in the methods and assays of the invention may be prepared by any available method or process.

Methods of isolating total mRNA are well known to those of skill in the art. For example, methods of isolation and purification of nucleic acids are described in detail in Chapter 3 of Laboratory Techniques in Biochemistry and Molecular Biology, Vol. 24, Hybridization With Nucleic Acid Probes: Theory and Nucleic Acid Probes, P. Tijssen, Ed. , Elsevier Press, New York, 1993. Such samples include RNA samples, but also include cDNA synthesized from a mRNA sample isolated from a cell or tissue of interest. Such samples also include DNA amplified from the cDNA, and RNA transcribed from the amplified DNA. One of skill in the art would appreciate that it is desirable to inhibit or destroy RNase present in homogenates before homogenates are used.

[00180] Biological samples may be of any biological tissue or fluid or cells from any organism as well as cells raised in vitro, such as cell lines and tissue culture cells.

Frequently the sample will be a tissue or cell sample that has been exposed to a compound, agent, drug, pharmaceutical composition, potential environmental pollutant or other composition. In some formats, the sample will be a"clinical sample"which is a sample derived from a patient. Typical clinical samples include, but are not limited to, sputum, blood, blood-cells (e. g., white cells), tissue or fine needle biopsy samples, urine, peritoneal fluid, and pleural fluid, or cells therefrom. Biological samples may also include sections of tissues, such as frozen sections or formalin fixed sections taken for histological purposes.

Forming High Density Arrays [00181] Methods of forming high density arrays of oligonucleotides with a minimal number of synthetic steps are known. The oligonucleotide analogue array can be synthesized on a single or on multiple solid substrates by a variety of methods, including, but not limited to, light-directed chemical coupling, and mechanically directed coupling (see Pirrung, U. S. Patent No. 5,143, 854).

[00182] In brief, the light-directed combinatorial synthesis of oligonucleotide arrays on a glass surface proceeds using automated phosphoramidite chemistry and chip masking techniques. In one specific implementation, a glass surface is derivatized with a silane reagent containing a functional group, e. g., a hydroxyl or amine group blocked by a photolabile protecting group. Photolysis through a photolithographic mask is used selectively to expose functional groups which are then ready to react with incoming 5' photoprotected nucleoside phosphoramidites. The phosphoramidites react only with those sites which are illuminated (and thus exposed by removal of the photolabile blocking group). Thus, the phosphoramidites only add to those areas selectively exposed from the preceding step. These steps are repeated until the desired array of sequences have been synthesized on the solid surface. Combinatorial synthesis of different oligonucleotide analogues at different locations on the array is determined by the pattern of illumination during synthesis and the order of addition of coupling reagents.

[00183] In addition to the foregoing, additional methods which can be used to generate an array of oligonucleotides on a single substrate are described in PCT Publication Nos. WO 93/09668 and WO 01/23614. High density nucleic acid arrays can also be fabricated by depositing pre-made or natural nucleic acids in predetermined positions. Synthesized or natural nucleic acids are deposited on specific locations of a substrate by light directed targeting and oligonucleotide directed targeting. Another embodiment uses a dispenser that moves from region to region to deposit nucleic acids in specific spots.

Hybridization [00184] Nucleic acid hybridization simply involves contacting a probe and target nucleic acid under conditions where the probe and its complementary target can form stable hybrid duplexes through complementary base pairing. See WO 99/32660. The nucleic acids that do not form hybrid duplexes are then washed away leaving the hybridized nucleic acids to be detected, typically through detection of an attached detectable label. It is generally recognized that nucleic acids are denatured by increasing the temperature or decreasing the salt concentration of the buffer containing the nucleic acids. Under low stringency conditions (e. g., low temperature and/or high salt) hybrid duplexes (e. g., DNA: DNA, RNA: RNA, or RNA: DNA) will form even where the annealed sequences are not perfectly complementary. Thus, specificity of hybridization is reduced at lower stringency.

Conversely, at higher stringency (e. g., higher temperature or lower salt) successful hybridization tolerates fewer mismatches. One of skill in the art will appreciate that hybridization conditions may be selected to provide any degree of stringency.

[00185] In a preferred embodiment, hybridization is performed at low stringency, in this case in 6x SSPET at 37°C (0.005% Triton X-100), to ensure hybridization and then subsequent washes are performed at higher stringency (e. g., Ix SSPET at 37°C) to eliminate mismatched hybrid duplexes. Successive washes may be performed at increasingly higher stringency (e. g., down to as low as 0.25x SSPET at 37°C to 50°C) until a desired level of hybridization specificity is obtained. Stringency can also be increased by addition of agents such as formamide. Hybridization specificity may be evaluated by comparison of hybridization to the test probes with hybridization to the various controls that can be present (e. g. , expression level control, normalization control, mismatch controls, etc.).

[00186] In general, there is a tradeoff between hybridization specificity (stringency) and signal intensity. Thus, in a preferred embodiment, the wash is performed at the highest stringency that produces consistent results and that provides a signal intensity greater than approximately 10% of the background intensity. Thus, in a preferred embodiment, the hybridized array may be washed at successively higher stringency solutions and read between each wash. Analysis of the data sets thus produced will reveal a wash stringency above which the hybridization pattern is not appreciably altered and which provides adequate signal for the particular oligonucleotide probes of interest.

Signal Detection [00187] The hybridized nucleic acids are typically detected by detecting one or more labels attached to the sample nucleic acids. The labels may be incorporated by any of a number of means well known to those of skill in the art. See WO 99/32660.

Databases [00188] The present invention includes relational databases containing sequence information, for instance, for the genes of Tables 1-SN, as well as gene expression or related information from tissue or cells exposed to various standard toxins, such as those herein described (see Tables 5A-5N). Databases may also contain information associated with a given sequence or tissue sample such as descriptive information about the gene associated with the sequence information (see Tables 1 and 2), or descriptive information concerning the clinical status of the tissue sample, or the animal from which the sample was derived.

The database may be designed to include different parts, for instance a sequence database and a gene expression database. Methods for the configuration and construction of such databases and computer-readable media to which such databases are saved are widely available, for instance, see U. S. Publication No. 2003-0171876 (Serial No. 10/090,144), filed March 5,2002, PCT Publication No. WO 02/095659, published November 23,2002, and U. S. Patent No. 5,953, 727, which are herein incorporated by reference in their entirety.

In a preferred embodiment, the database is ToxExpress marketed by Gene Logic, Inc., Gaithersburg, MD.

[00189] The databases of the invention may be linked to an outside or external database such as GenBank (www. ncbi. nlm. nih. gov/entrez. index. html) ; KEGG (www. genome. ad. jp/kegg) ; SPAD (www. grt. kyushu-u. acjplspadlindex. html) ; HUGO (www. gene. ucl. ac. uklhugo) ; Swiss-Prot (www. expasy. ch. sprot) ; Prosite (www. expasy. chltoolslscnpsitl. html) ; OMIM (www. ncbi. nlm. nih. govlomim) ; and GDB (www. gdb. org). In a preferred embodiment, as described in Tables 1-5N, the external database is GenBank and the associated databases maintained by the National Center for Biotechnology Information (NCBI) (www. ncbi. nlm. nih. gov).

[00190] Any appropriate computer platform, user interface, etc. may be used to perform the necessary comparisons between sequence information, gene expression information and any other information in the database or information provided as an input. For example, a large number of computer workstations are available from a variety of manufacturers.

Client/server environments, database servers and networks are also widely available and appropriate platforms for the databases of the invention.

[00191] The databases of the invention may be used to produce, among other things, electronic Northerns (E-NORTHERN, Gene Logic, Inc. , Gaithersburg, MD) that allow the user to determine the cell type or tissue in which a given gene is expressed and to allow determination of the abundance or expression level of a given gene in a particular tissue or cell.

[00192] The databases of the invention may also be used to present information identifying the expression level in a tissue or cell of a set of genes comprising one or more of the genes in Tables 1-5N, comprising the step of comparing the expression level of at least one gene in Tables 1-5N in a cell or tissue exposed to a test agent to the level of expression of the gene in the database. In one embodiment, such methods may be used to predict the toxic potential of a given compound by comparing the level of expression of a gene or genes in Tables 1-5N from a tissue or cell sample exposed to the test agent to the expression levels found in a control tissue or cell samples exposed to a standard toxin or renal toxin such as those herein described. Such methods may also be used in the drug or agent screening assays as described herein.

Kits [00193] The invention further includes kits combining, in different combinations, high- density oligonucleotide arrays, reagents for use with the arrays, protein reagents encoded by the genes of the Tables, signal detection and array-processing instruments, gene expression databases and analysis and database management software described above. The kits may be used, for example, to predict or model the toxic response of a test compound, to monitor the progression of renal disease states, to identify genes that show promise as new drug targets and to screen known and newly designed drugs as discussed above.

[00194] The databases packaged with the kits are a compilation of expression patterns from human or laboratory animal genes and gene fragments (corresponding to the genes of Tables 1-5N). In particular, the database software and packaged information that may contain the databases saved to a computer-readable medium include the expression results of Tables 1-5N that can be used to predict toxicity of a test agent by comparing the expression levels of the genes of Tables 1-5N induced by the test agent to the expression levels presented in Tables 5A-5N. In another format, database and software information may be provided in a remote electronic format, such as a website, the address of which may be packaged in the kit.

[00195] The kits may used in the pharmaceutical industry, where the need for early drug testing is strong due to the high costs associated with drug development, but where bioinformatics, in particular gene expression informatics, is still lacking. These kits will reduce the costs, time and risks associated with traditional new drug screening using cell cultures and laboratory animals. The results of large-scale drug screening of pre-grouped patient populations, pharmacogenomics testing, can also be applied to select drugs with greater efficacy and fewer side-effects. The kits may also be used by smaller biotechnology companies and research institutes who do not have the facilities for performing such large- scale testing themselves.

[00196] Databases and software designed for use with microarrays are discussed in Balaban et al., U. S. Patent Nos. 6,229, 911, a computer-implemented method for managing information, stored as indexed Tables 1-5N, collected from small or large numbers of microarrays, and 6,185, 561, a computer-based method with data mining capability for collecting gene expression level data, adding additional attributes and reformatting the data to produce answers to various queries. Chee et al., U. S. Patent No. 5,974, 164, disclose a software-based method for identifying mutations in a nucleic acid sequence based on differences in probe fluorescence intensities between wild type and mutant sequences that hybridize to reference sequences.

[00197] Without further description, it is believed that one of ordinary skill in the art can, using the preceding description and the following illustrative examples, make and utilize the compounds of the present invention and practice the claimed methods. The following working examples therefore, specifically point out the preferred embodiments of the present invention, and are not to be construed as limiting in any way the remainder of the disclosure.

EXAMPLES Example 1: Identification Of Toxicity Markers Using Linear Discriminant Analysis (LDA) [00198] The renal toxins indomethacin, diflunisal, colchicine, chloroform, diclofenac, menadione, sodium chromate, sodium oxalate, thioacetamide, vancomycin, acyclovir, adriamycin, AY-25329, bromoethylamine HBr (BEA), carboplatin, carbon tetrachloride, cephalosporine, cidofovir, cisplatin, citrinin, cyclophosphamide, cyclosporine, gentamicin, hexachloro-1, 3-butadiene, hydralazine, ifosfamide, lithium chloride, mercuric chloride, pamindronate, puromycin aminonucleoside (PAN), semustine and sulfadiazine were administered to male Sprague-Dawley rats at various timepoints using administration diluents, protocols and dosing regimes as previously described in the art and previously described in the priority applications discussed above. As negative controls, the compounds ceftazidime, streptomycin, transplatin captopril, phenobarbital, tamoxifen and temozolomide were used. In experiments using toxins A-G, as labeled in Table 4, blood and tissue samples were collected at the following time-points: chloroform (A), thioacetamide (F) and vancomycin (G) -after 6,24 and 48 hours of exposure; diclofenac (B) and menadione (C) -after 3,6 and 24 hours of exposure; and sodium chromate (D) and sodium oxalate (E) -after 6,24 and 72 hours of exposure. For these compounds, no significant changes in the levels of gene expression were found with varying exposure time, i. e. , short and long time-points showed the same pattern of differential gene expression.

The low and high dose level for each compound are provided in the chart below.

[00199] Renal Toxin Low Dose (mg/kg) High Dose (mg/kg) Method of Administration indomethacin 10 oral gavage diflunisal 2 400 oral gavage colchicine 0. 15 1. 5 intraperitoneal chloroform 11. 95 239 oral gavage diclofenac 1 200 intraperitoneal menadione 15 150 intravenous sodium chromate 3 30 intraperitoneal sodium oxalate 10 100 intraperitoneal thioacetamide 30 300 intraperitoneal vancomycin 50 500 intravenous [00200] For the remaining compounds, the doses and methods of administration used were as follows: Renal Toxin Low Dose High Dose Method of (mg/kg) (mg/kg) Administration cephaloridine 100 800 intravenous cisplatin intravenous PAN 10 150 intravenous BEA 10 200 intraperitoneal gentamicin 2 80 intramuscular ifosfamide 5 100 intra eritoneal cyclophosphamide 20 2000 intraperitoneal carboplatin 5 50 intravenous AY-25329 25 250 oral gavage indomethacin 1 10 oral gavage acyclovir 10 100 intraperitoneal citrinin 1 35 intraperitoneal mercuric chloride 0. 1 1 intravenous diflunisal 2 400 oral gavage cidofovir 10 100 intraperitoneal pamidronate 1 60 intraperitoneal lithium 0. 3 (nmol/kg) 3 (nmol/kg) intraperitoneal Renal Toxin Low Dose High Dose Method of (mg/kg) (mg/kg) Administration hydralazine 2. 5 25 intraperitoneal colchicine 0. 15 1. 5 intraperitoneal sulfadiazine 100 1000 intravenous adriamycin 1.3 12. 8 intravenous Animals were sacrificed and samples collected at the time points previously described in the priority applications discussed above.

[00201] After administration, the dosed animals were observed and tissues were collected as described below: OBSERVATION OF ANIMALS [00202] 1. Clinical cage side observations-twice daily mortality and moribundity check.

Skin and fur, eyes and mucous membrane, respiratory system, circulatory system, autonomic and central nervous system, somatomotor pattern, and behavior pattern were checked. Potential signs of toxicity, including tremors, convulsions, salivation, diarrhea, lethargy, coma or other atypical behavior or appearance, were recorded as they occurred and included a time of onset, degree, and duration.

[00203] 2. Physical Examinations-Prior to randomization, prior to initial treatment, and prior to sacrifice.

[00204] 3. Body Weights-Prior to randomization, prior to initial treatment, and prior to sacrifice.

CLINICAL PATHOLOGY [00205] 1. Frequency-Prior to necropsy.

[00206] 2. Number of animals-All surviving animals.

[00207] 3. Bleeding Procedure-Blood was obtained by puncture of the orbital sinus while under 70% C02/30% 02 anesthesia.

[00208] 4. Collection of Blood Samples-Approximately 0.5 mL of blood was collected into EDTA tubes for evaluation of hematology parameters. Approximately 1 mL of blood was collected into serum separator tubes for clinical chemistry analysis. Approximately 200 uL of plasma was obtained and frozen at-80°C for test compound/metabolite estimation.

An additional-2 mL of blood was collected into a 15 mL conical polypropylene vial to which-3 mL of Trizol was immediately added. The contents were immediately mixed with a vortex and by repeated inversion. The tubes were frozen in liquid nitrogen and stored at - 80°C.

TERMINATION PROCEDURES Terminal Sacrifice [00209] Approximately 3,6, 24,48, 72,120, 144,168, 336, and/or 360 hours after the initial dose, rats were weighed, physically examined, sacrificed by decapitation, and exsanguinated. The animals were necropsied within approximately five minutes of sacrifice. Separate sterile, disposable instruments were used for each animal, with the exception of bone cutters, which were used to open the skull cap. The bone cutters were dipped in disinfectant solution between animals.

[00210] Necropsies were conducted on each animal following procedures approved by board-certified pathologists.

[00211] Animals not surviving until terminal sacrifice were discarded without necropsy (following euthanasia by carbon dioxide asphyxiation, if moribund). The approximate time of death for moribund or found dead animals was recorded.

Postmortem Procedures [00212] Fresh and sterile disposable instruments were used to collect tissues. Gloves were worn at all times when handling tissues or vials. All tissues were collected and frozen within approximately 5 minutes of the animal's death. The liver sections and kidneys were frozen within approximately 3-5 minutes of the animal's death. The time of euthanasia, an interim time point at freezing of liver sections and kidneys, and time at completion of necropsy were recorded. Tissues were stored at approximately-80°C or preserved in 10% neutral buffered formalin.

Tissue Collection and Processing [002131 Liver 1. Right medial lobe-snap frozen in liquid nitrogen and stored at-80°C.

2. Left medial lobe-Preserved in 10% neutral-buffered formalin (NBF) and evaluated for gross and microscopic pathology.

3. Left lateral lobe-snap frozen in liquid nitrogen and stored at-80°C.

[00214] Heart-A sagittal cross-section containing portions of the two atria and of the two ventricles was preserved in 10% NBF. The remaining heart was frozen in liquid nitrogen and stored at--80°C.

[00215] Kidneys (both) 1. Left-Hemi-dissected; half was preserved in 10% NBF and the remaining half was frozen in liquid nitrogen and stored at--80°C.

2. Right-Hemi-dissected; half was preserved in 10% NBF and the remaining half was frozen in liquid nitrogen and stored at--80°C.

[00216] Testes (both) -A sagittal cross-section of each testis was preserved in 10% NBF.

The remaining testes were frozen together in liquid nitrogen and stored at-80°C.

[00217] Brain (whole) -A cross-section of the cerebral hemispheres and of the diencephalon was preserved in 10% NBF, and the rest of the brain was frozen in liquid nitrogen and stored at--80°C.

[00218] Microarray sample preparation was conducted with minor modifications, following the protocols set forth in the Affymetrix GeneChips Expression Technical Analysis Manual (Affymetrix, Inc. Santa Clara, CA). Frozen tissue was ground to a powder using a Spex Certiprep 6800 Freezer Mill. Total RNA was extracted with Trizol (Invitrogen, Carlsbad CA) utilizing the manufacturer's protocol. The total RNA yield for each sample was 200- 500 g per 300 mg tissue weight. mRNA was isolated using the Oligotex mRNA Midi kit (Qiagen) followed by ethanol precipitation. Double stranded cDNA was generated from mRNA using the SuperScript Choice system (Invitrogen, Carlsbad CA). First strand cDNA synthesis was primed with a T7- (dT24) oligonucleotide. The cDNA was phenol-chloroform extracted and ethanol precipitated to a final concentration of 1 pg/ml. From 2 gg of cDNA, cRNA was synthesized using Ambion's T7 MegaScript in vitro Transcription Kit.

[00219] To biotin label the cRNA, nucleotides Bio-11-CTP and Bio-16-UTP (Enzo Diagnostics) were added to the reaction. Following a 37°C incubation for six hours, impurities were removed from the labeled cRNA following the RNeasy Mini kit protocol (Qiagen). cRNA was fragmented (fragmentation buffer consisting of 200 mM Tris-acetate, pH 8.1, 500 mM KOAc, 150 mM MgOAc) for thirty-five minutes at 94°C. Following the Affymetrix protocol, 55 llg of fragmented cRNA was hybridized on the Affymetrix rat array set for twenty-four hours at 60 rpm in a 45°C hybridization oven. The chips were washed and stained with Streptavidin Phycoerythrin (SAPE) (Molecular Probes) in Affymetrix fluidics stations. To amplify staining, SAPE solution was added twice with an anti- streptavidin biotinylated antibody (Vector Laboratories) staining step in between.

Hybridization to the probe arrays was detected by fluorometric scanning (Hewlett Packard Gene Array Scanner). Data was analyzed using Affymetrix GeneChipX version 2.0 and Expression Data Mining (EDMT) software (version 1.0), the GeneExpress database, and S-Plus statistical analysis software (Insightful Corp.).

[00220] Tables 1 and 2 disclose those genes that are differentially expressed upon exposure to the named toxins and their corresponding GenBank Accession and Sequence Identification numbers, the identities of the metabolic pathways in which the genes function, the gene names if known, and the unigene cluster titles. The model code represents the various toxicity state that each gene is able to discriminate as well as the individual toxin type associated with each gene. The codes are defined in Table 4. The GLGC ID is the internal Gene Logic identification number.

[00221] Table 3 discloses those genes that are the human homologues of those genes in Tables 1 and 2 that are differentially expressed upon exposure to the named toxins. The corresponding GenBank Accession and Sequence Identification numbers, the gene names if known, and the unigene cluster titles of the human homologues are listed.

[00222] Table 4 defines the models of Tables 5A-5N.

[00223] The models of Tables 5A-5M (individual toxin models, pathology models and general toxin models) disclose the summary statistics for each of the comparisons performed. Table 5A contains gene expression information from the chloroform toxicity model. Table 5B contains gene expression information from the diclofenac toxicity model.

Table C contains gene expression information from the menadione toxicity model. contains gene expression information from the chloroform toxicity model. Table D contains gene expression information from the sodium chromate toxicity model. Table E contains gene expression information from the sodium oxalate toxicity model. Table F contains gene expression information from the thioacetamide toxicity model. Table G contains gene expression information from the vancomycin toxicity model. Table H contains gene expression information from the pathology model of damage to the S2 segment of the renal proximal tubule. Table I contains gene expression information from the pathology model of renal tubular toxicity. Table J contains gene expression information from the pathology model of glomerular injury. Table K contains gene expression information from the pathology model of tubular obstruction. Table L contains gene expression information from the NSAIDS (non-steroidal anti-inflammatory drugs) toxicity model. Lastly, Table M contains gene expression information from a general toxicity model.

[00224] Each of these tables contains a set of predictive genes and creates a model for predicting the renal toxicity of an unknown, i. e. , untested compound. Each gene is identified by its Gene Logic identification number and can be cross-referenced to a gene name and representative SEQ ID NO. in Tables 1 and 2. For each comparison of gene expression levels between samples in the toxicity group (samples affected by exposure to a specific toxin) and samples in the non-toxicity group (samples not affected by exposure to that same specific toxin), the tox group mean (for toxicity group samples) is the mean signal intensity, as normalized for the various chip parameters that are being assayed. The non-tox group mean represents the mean signal intensity, as normalized for the various chip parameters that are being assayed, in samples from animals other than those treated with the high dose of the specific toxin. These animals were treated with a low dose of the specific toxin, or with vehicle alone, or with a different toxin. Samples in the toxicity groups were obtained from animals sacrificed at the time points previously described, while samples in the non-toxicity groups were obtained from animals sacrificed at all time points in the experiments. For individual genes, an increase in the tox mean compared to the non-tox mean indicates up-regulation upon exposure to a toxin. Conversely, a decrease in the tox mean compared to the non-tox mean indicates down-regulation.

[00225] The mean values are derived from Average Difference (AveDiff) values for a particular gene, averaged across the corresponding samples. Each individual Average Difference value is calculated by integrating the intensity information from multiple probe pairs that are tiled for a particular fragment. The normalization multiplies each expression intensity for a given experiment (chip) by a global scaling factor. The intent of this normalization is to make comparisons of individual genes between chips possible. The scaling factor is calculated as follows: [00226] 1. From all the unnormalized expression values in the experiment, delete the largest 2% and smallest 2% of the values. That is, if the experiment yields 10,000 expression values, order the values and delete the smallest 200 and the largest 200.

2. Compute the trimmed mean, which is equal to the mean of the remaining values.

3. Compute the scale factor SF = 100/ (trimmed mean).

[00227] The value of 100 used here is the standard target value used. Some AveDiff values may be negative due to the general noise involved in nucleic acid hybridization experiments. Although many conclusions can be made corresponding to a negative value on the GeneChip platform, it is difficult to assess the meaning behind the negative value for individual fragments. Our observations show that, although negative values are observed at times within the predictive gene set, these values reflect a real biological phenomenon that is highly reproducible across all the samples from which the measurement was taken. For this reason, those genes that exhibit a negative value are included in the predictive set. It should be noted that other platforms of gene expression measurement may be able to resolve the negative numbers for the corresponding genes. The predictive ability of each of those genes does extend across platforms. Each mean value is accompanied by the standard deviation for the mean. The linear discriminant analysis score (discriminant score), as disclosed in the tables, measures the ability of each gene to predict whether or not a sample is toxic. The discriminant score is calculated by the following steps: Calculation of a discriminant score [00228J 1. Let Xi represent the AveDiff values for a given gene across the non-tox samples, i=l... n.

2. Let Yi represent the AveDiff values for a given gene across the tox samples, i=1... t.

The calculations proceed as follows: 3. Calculate mean and standard deviation for Xi's and Ys's, and denote these by mx, my, Sx, SY.

4. For all Xj's and Yi's, evaluate the function f (z) = ((l/sy) *exp (-. 5* ((z-my)/sy) 2))/ ( ( (l/sy) *exp (-. 5* ( (z-mY)/sY) 2)) + ((llsx) *exp (-. 5*((z-mx)/sx)2))).

5. The number of correct predictions, say P, is then the number of Ys's such that f (Ys) >. 5 plus the number of Xi's such that f (Xi) <. 5.

6. The discriminant score is then P/ (n+t).

[00229] Linear discriminant analysis uses both the individual measurements of each gene and the calculated measurements of all combinations of genes to classify samples. For each gene a weight is derived from the mean and standard deviation of the toxic and nontox groups. Every gene is multiplied by a weight and the sum of these values results in a collective discriminate score. This discriminant score is then compared against collective centroids of the tox and nontox groups. These centroids are the average of all tox and nontox samples respectively. Therefore, each gene contributes to the overall prediction.

This contribution is dependent on weights that are large positive or negative numbers if the relative distances between the tox and nontox samples for that gene are large and small numbers if the relative distances are small. The discriminant score for each unknown sample and centroid values can be used to calculate a probability between zero and one as to the group in which the unknown sample belongs.

Example 2: Identification of Toxicity Markers Using RMA and PLS Algorithms [00230] Dosing of animals with toxins and vehicle controls, sacrificing of animals, preparation and hybridization of RNA to DNA microarrays, and obtaining gene expression values were performed as described in Example 1 above. The following toxins and negative controls were used and administered according to the protocols in Table 6.

[00231] RMA/PLS models were built as follows. From DNA microarray data from one or more tox studies, a matrix of RMA fold-change expression values was generated. These values may be generated, for example, according to the method of Irizarry et al. (Nucl Acids Res 31 (4): el5, 2003), which uses the following equation to produce a log scale linear additive model: T (PM*j) = e ; + a + £ ; . T represents the transformation that corrects for background and normalizes and converts the PM (perfect match) intensities to a log scale. ei represents the log2 scale expression values found on arrays i = 1-1, aj represents the log scale affinity effects for probes j = 1-J, and Eij represents error (to correct for the differences in variances when using probes that bind with different intensities). In RMA fold-change matrices, the rows represent individual fragments, and the columns are individual samples. A vehicle cohort median matrix was then calculated, in which the rows represent fragments and the columns represent vehicle cohorts, one cohort for each study/time-point combination. The values in this matrix are the median RMA expression values across the samples within those cohorts. Next, a matrix of normalized RMA expression values was generated, in which the rows represent individual fragments and the columns are individual samples. The normalized RMA values are the RMA values minus the value from the vehicle cohort median matrix corresponding to the time-matched vehicle cohort. PLS modeling was then applied to the normalized RMA matrix (a subset by taking certain fragments as described below), using a-1 = non-tox, +1 = tox supervised score vector.

[00232] To select fragments, a vehicle cohort mean matrix was generated, in which the rows represent fragments and the columns represent vehicle cohorts, one cohort for each study/time-point combination. The values in this matrix are the mean RMA expression values across the samples within those cohorts. A treated cohort mean matrix was then generated, in which the rows represent fragments and the columns represent treated (non- vehicle) cohorts, one cohort for each study/time-point/compound/dose combination. The values in this matrix are the mean RMA expression values across the samples within those cohorts. Next, a treated cohort fold-change matrix was generated, in which the rows represent fragments and the columns represent treated cohorts, one cohort for each study/time-point/compound/dose combination. The values in this matrix are the values in the treated cohort mean matrix minus the values in the vehicle cohort mean matrix corresponding to appropriate time-matched vehicle cohorts. Subsequently, a treated cohort p-value matrix was generated, in which the rows represent fragments and the columns represent treated cohorts, one cohort for each study/time-point/compound/dose combination. The values in this matrix are p-values based on two-sample t-tests comparing the treated cohort mean values to the vehicle cohort mean values corresponding to appropriate time-matched vehicle cohorts. This matrix was converted to a binary coding based on the p-values being less than 0.05 (coded as 1) or greater than 0.05 (coded as 0).

[00233] The row sums of the binary treated cohort p-value matrix were computed, where that row sum represents a"regulation score"for each fragment, representing the total number of treated cohorts where the fragment showed differential regulation (up-or down- regulation) compared to its time-matched vehicle cohort. PLS modeling and cross- validation were then performed based on taking the top N fragments according to the regulation score, varying N and recording the model success rate for each N. N was chosen to be the point at which the cross-validated error rate was minimized. In the PLS model, each of those N fragments receives a PLS weight (PLS score) corresponding to the fragment's utility, or predictive ability, in the model. The data in Table 5N are taken from a kidney toxicity prediction model in which 2179 samples were assayed. This predictive model is based on expression levels of 782 genes. Thus, using a set of genes and a supervised grouping of samples, PLS can identify optimal prediction weights for those genes.

[00234] To determine whether or not a sample from an animal treated with a test compound shows a toxic response, RNA is prepared from a treatment sample and hybridized to a DNA microarray, as described in Example 1 above. From the gene expression information, a prediction score is calculated for that sample and compared to a reference score from a kidney toxicity reference database according to the following equation. The sample prediction score = Y-wi RFCi."i"is the index number for each gene in a gene expression profile to be evaluated."ws"is the PLS weight (or PLS score, see Table 5N) for each gene.

"RFC"'is the RMA fold-change value for the ith gene, as determined from a normalized RMA matrix of gene expression data from the sample (described above). The PLS weight multiplied by the RMA fold-change value gives a prediction score for each gene, and the prediction scores for all the individual genes are added to give a prediction score for the sample. In a kidney toxicity database of the instant invention, a cut-off prediction score is about 0.318. If the sample score is about 0.318 or above, it can be predicted that the sample shows a toxic response after exposure to the test compound. If the sample score is below 0.318, it can be predicted that the sample does not show a toxic response.

[00235] The model can be trained by setting a score of-1 for each gene that cannot predict a toxic response and by setting a score of +1 for each gene that can predict a toxic response.

Cross-validation of RMA/PLS models was performed by the compound-drop method and by the 2/3: 1/3 method. In the compound-drop method, sample data from animals treated with one particular test compound were removed from a model, and the ability of this model to predict toxicity was compared to that of a model containing a full data set. In the 2/3: 1/3 method, gene expression information from a random third of the genes in the model was removed, and the ability of this subset model to predict toxicity was compared to that of a model containing a full data set.

[00236] Compared to LDA models for predicting kidney toxicity, RMA/PLS models showed about a 10% increase in the true positive sample rates (89% vs. 79%) and about a 1.5% increase in the false positive sample rates (2.5% vs. 1%).

Example 3: General Toxicity Modeling [00237] Samples were selected for grouping into tox-responding and non-tox-responding groups by examining each study individually with Principal Components Analysis (PCA) to determine which treatments had an observable response. Only groups where confidence of their tox-responding and non-tox-responding status was established were included in building a general tox model (Table 5M).

[00238] Linear discriminant models were generated to describe toxic and non-toxic samples. The top discriminant genes and/or EST's were used to determine toxicity by calculating each gene's contribution with homo and heteroscedastic treatment of variance and inclusion or exclusion of mutual information between genes. Prediction of samples within the database exceeded 80% true positives with a false positive rate of less than 5%.

It was determined that combinations of genes and/or EST's generally provided a better predictive ability than individual genes and that the more genes and/or EST used the better predictive ability. Although the preferred embodiment includes fifty or more genes, many pairings or greater combinations of genes and/or EST can work better than individual genes.

All combinations of two or more genes from the selected list (Table 5M) could be used to predict toxicity. These combinations could be selected by pairing in an agglomerate, divisive, or random approach. Further, as yet undetermined genes and/or EST's could be combined with individual or combination of genes and/or EST's described here to increase predictive ability. However, the genes and/or EST's described here would contribute most of the predictive ability of any such undetermined combinations.

[00239] Other variations on the above method can provide adequate predictive ability.

These include selective inclusion of components via agglomerate, divisive, or random approaches or extraction of loading and combining them in agglomerate, divisive, or random approaches. Also the use of composite variables in logistic regression to determine classification of samples can also be accomplished with linear discriminate analysis, neural or Bayesian networks, or other forms of regression and classification based on categorical or continual dependent and independent variables.

Example 4: Modeling Methods [00240] The above modeling methods provide broad approaches of combining the expression of genes to predict sample toxicity. One could also provide no weight in a simple voting method or determine weights in a supervised or unsupervised method using agglomerate, divisive, or random approaches. All or selected combinations of genes may be combined in ordered, agglomerate, or divisive, supervised or unsupervised clustering algorithms with unknown samples for classification. Any form of correlation matrix may also be used to classify unknown samples. The spread of the group distribution and discriminate score alone provide enough information to enable a skilled person to generate all of the above types of models with accuracy that can exceed discriminate ability of individual genes. Some examples of methods that could be used individually or in combination after transformation of data types include but are not limited to: Discriminant Analysis, Multiple Discriminant Analysis, logistic regression, multiple regression analysis, linear regression analysis, conjoint analysis, canonical correlation, hierarchical cluster analysis, k-means cluster analysis, self-organizing maps, multidimensional scaling, structural equation modeling, support vector machine determined boundaries, factor analysis, neural networks, bayesian classifications, and resampling methods. Further, in any model, a compound may be classified as a negative control because it appears to produce reduced toxicity, although the compound may be added to the model as a toxin to increase the sensitivity for predicting toxicity.

Example 5: Grouping Of Individual Compound And Pathology Classes [00241] Samples were grouped into individual pathology classes based on known toxicological responses and observed clinical chemical and pathology measurements or into early and late phases of observable toxicity within a compound (Tables 5A-5L). The top 10,25, 50, 100 genes based on individual discriminate scores were used in a model to ensure that combination of genes provided a better prediction than individual genes. As described above, all combinations of two or more genes from this list could potentially provide better prediction than individual genes when selected in any order or by ordered, agglomerate, divisive, or random approaches. In addition, combining these genes with other genes could provide better predictive ability, but most of this predictive ability would come from the genes listed herein.

[00242] Samples may be considered toxic if they score positive in any pathological or individual compound class represented here or in any modeling method mentioned under general toxicology models based on combination of individual time and dose grouping of individual toxic compounds obtainable from the data. The pathological groupings and early and late phase models are preferred examples of all obtainable combinations of sample time and dose points. Most logical groupings with one or more genes and one or more sample dose and time points should produce better predictions of general toxicity, pathological specific toxicity, or similarity to known toxicant than individual genes.

[00243] Although the present invention has been described in detail with reference to examples above, it is understood that various modifications can be made without departing from the spirit of the invention. Accordingly, the invention is limited only by the following claims. All cited patents, patent applications and publications referred to in this application are herein incorporated by reference in their entirety.

Table 1 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Title Ratlus norvegicus transcribed sequence with strong similarity to protein reff:NP_112456.1 (M.musculus) splicing factor 3b, subunit 1, 155 kDa (Mus 6917 1 AA012709 B nusculus) 25098 2 AA108277 N,C,H Rattus norvegicus transcribed sequence with strong similarity to protein pir:T30827 *M.musculus) T30827 nascent polypeptide-associated complex 6049 3 AA685178 F alpha chain, non-muscle splice form - mouse Rattus norvegicus transcribed sequence with strong similarity to prolein sp:Q93068 (M.musculus) SM33_HUMAN Ubiquitin-like protein SMT3C precursor (Ubiquitinp-homology domain protein PIC1) (Ubiquitin-like protein UBL1) (Ubiquitin-related protein SUMO-1) (GAP modifying protein 1) (GBP1) 25106 4 AA6886579 8 (Sentrin) ATPase, CA++ transporting, cardiac muscle, slow twitch 12349 5 AA799276 M 2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 Rattus norvegicus transcribed sequence with strong similarity to protein ref:NP_062732.1 (M.musculus) mitochondrial carrier homolog 2 [Mus 19222 6 AA799279 J musculus] Rattus norvegicus transcribed sequence with moderate similarity to protein 18272 7 aA799294 I ref:NP_)55993.1 (H.sapiens) KIAA0717 protein [Homo sapiens] Rattus norvegicus transcribed sequence with strong similarity to protein ref:NP_057030.1 (H.sapiens) CGI-17 protein, pelota (Drosophila) homolog 18396 8 AA799330 M,N,H,I [Homo sapiens] 16039 9 AA799452 H transldolase 1 transaldolase 1 20961 10 AA799465 L Rattus norvegicus transcribed sequence 16150 11 AA799489 G acyl-coA oxidase acyl-coA oxidase 18291 12 AA799497 N Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with moderate similarity to prolein 15302 13 AA799518 M ref:NP_075223.1 (R.norvegicus) DnaJ-like protein [Rattus norvegicus] Rattus norvegicus transcribed sequence with moderate similarity to protein 15303 13 AA799518 F ref:NP_)75223.1 (R.norvegicus) DnaJ-like [Rattus norvegicus] 23063 14 AA799534 M,N,K Rattus norvegicus transcribed sequences 22669 15 AA799567 D Rattus norvegicus transcribed sequences Table 1 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Title Rattus norvegicus transcribed sequence with strong similarity to protein 18361 16 AA799591 M,N prf:1202265A (R.norevegicus) 1202265A tubulin T beta15 [Rattus norvegicus] Rattus norvegicus transcribed sequence with strong similarity to protein ref:NP_115647.1 (H.sapiens) hypothetical protein DKFZp5861021 [Homo 15844 17 AA799600 D sapiens] Rattus norvegicus transcribed sequence with strong similarity to protein ref:NP_038936.1 (M.musculus) f-box and WD-40 domain protein 5; F-box 22910 18 AA799654 K protein Fbw5 [Mus musculus] 14309 19 AA799676 M,N Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with weak similarity to protein ref:NP_476544.1 (R.norvegicus) brain-specific angiogenesis inhibitor 1- 17494 20 AA799751 M,K associated protein 2 [Rattus norvegicus] 18360 21 AA799771 M,I Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with strong similarity to protein 21007 22 AA799861 N sp:P70434 (M.musculus) IRF7_MOUSE interferon regulatory factor 7 (IRF-7) Rattus norvegicus transcribed sequence with moderate similarity to protein 23202 23 AA799971 M ref:NP_060761.1 (H.sapiens) hypothetical protein FLJ10986 [Homo sapiens] Rattus norvegicus transcribed sequence with moderate similarity to protein 23203 23 AA799971 M,N ref:NP_060761.1 (H.sapiens) hypothetical protein FLJ10986 [Homo sapiens] 21029 24 AA799981 C protein kinase C-eta protein kinase C-eta 2098 25 AA799995 C actin, beta actin, beta 4412 26 AA800005 N CD151 antigen CD151 antigen Rattus norvegicus transcribed sequence with strong similarity to protein ref:NP_542787.1 (H.sapiens) chromosome 20 open reading frame 163 21035 27 AA800025 N [Homo sapiens] 21072 28 AA800211 K pyridoxine 5-phosphate oxidase pyridoxine 5-phosphate oxidase Rattus norvegicus transcribed sequence with strong similarity to protein ref:NP_073183.1 (R.norvegicus) small GTP-binding protein rab5 [Rattus 21086 29 AA800305 D norvegicus] Table 1 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Tille Rattus norvegicus transcribed sequence with weak similarity to protein sp:P04041 (R.norvegicus) GSHC_RAT Gulathione peroxidase (GSHPX-1) 17325 30 AA800587 M,G,K (Cellular glutathione peroxidase) 13930 31 AA800613 M zinc finger protein 36 zinc finger protein 36 18462 32 AA800708 N Rattus norvegicus transcribed sequences 18564 33 AA800745 M aminolevulinate,delta-,dehydratase aminolevulinate,delta,-dehydratase 6595 34 AA800753 C Rattus norvegicus transcribewd sequences 21388 35 AA800771 C Rattus norvegicus transcribed sequences 12797 36 AA800790 D Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with moderate similarity to protein sp:P16636 (R.norvegicus) LYOX_RAT Protein-lysine 6-oxidase precursor 22386 37 AA800844 N,F (Lysyl oxidase) 15022 38 AA801029 N nuclear receptor subfamily 2, group F, member 6 nuclear receptor subfamily 2, group F, member 6 14600 39 AA801076 K Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with strong similarity to protein 23115 40 AA801165 A,F sp:P02262 (R.norvegicus) H2A1_RAT Histone H2A.1 15027 41 AA801212 D Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with moderate similarity to protein 7543 42 AA801395 M ref:NP_080242.1 (M.musculus) RIKEN cDNA 2310039H08 [Mus musculus] platelet-activating factor acetylhydrolase beta subunit 20753 43 AA801441 M,N,C,I (PAF-AH beta) platelet-activiting factor acetylhydrolase beta subunit (PAF-AH beta) 5930 44 AA817688 B Rattus norvegicus transcribed sequences 24237 45 AA817726 M Rattus norvegicus transcribed sequences 1650 46 AA817825 A Peptidylglycine alpha-amidating monooxygenase Peptidylglycine alpha-amidating monooxygenase 2109 47 AA817887 N,G profilin profilin Rattus norvegicus transcribed sequence with wak similarity to protein ref:NP_)79770.1 (M.musculus) similar to human ATP6C source AF36357.1 16907 48 AA817977 C [Mus musculus] Rattus norvegicus transcribed sequence with weak similarity to protein ref:NP_062213.1 (R.norvegicus) regulator of G-protein signaling 3 [Rattus 6675 49 AA817994 C norvegicus] 3016 50 AA818069 H polyubiqulin polybiqulin Table 1 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Title Rattus norvegicus transcribed sequence with strong similarity to protein pir:A55314 (H.saplens) A55314 glycine-tRNA ligase (EC 6.1.1.14) precursor 16756 51 AA818089 M,A,I [validatedf] - human 10983 52 AA818132 G Rattus norvegicus transcribed sequences 6014 53 AA818153 B,H Rattus norvegicus transcribed sequences Rattus norvegicus protein tyrosine phosphatase non-receptor type 13 6022 54 AA818197 E (Ptpn13), 3'UTR 11421 55 AA818199 E src associated in mitosis, 68 kDa src associated in mitosis, 68 kDa 17771 56 AA818224 M Rat mRNA for beta-tubulin T beta15 5923 57 AA818355 M,I Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with moderate similarity to protein ref:NP_149107.1 (H.sapiens) hypothetical protein MGC16714 [Homo 11610 58 AA818725 J sapiens] 4291 59 AA818741 M,I,J Rattus norvegicus transcribed sequences 4330 60 AA818747 M,B chemokine (C-X-C molif) ligand 12 chemokine (C-X-C molif) ligand 12 Rattus norvegicus trnascribed sequence with strong similarity to protein 19723 61 AA818761 M pir:A36370 (M.musculus) A36370 immediate-early protein pip92 - mouse 4952 62 AA818907 M,C Rattus norvegicus transcribed sequences 10985 63 AA818998 M,I Rattus norvegicus transcribed sequences 16958 64 AA819021 A 5863 65 AA819111 M,H,I Rattus norvegicus transcribed sequences 12684 66 AA819179 Rattus norvegicus transcribed sequences 9125 67 AA819338 N signal sequence receptor 4 signal sequence receptor 4 17824 68 AA819362 A Rattus norvegicus Ba1-643 mRNA, complete cds 6336 69 AA819403 M Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with strong similarity to protein 6287 70 AA819471 B ref:NP_079741.1 (M.musculus) RIKEN cDNA 1810030N24 [Mus musculus] 19433 71 AA81976 H Rattus norvegicus transcribed sequence with strong similarity to protein 22820 72 AA848315 M pir:JT0565 (M.musculus) JT0565 IMP dehydrogenase (EC 1.1.1.205) - mouse Table GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Title Rattus norvegicus transcribed sequence with weak similarity to protein ref:NP_496764.1 (C.elegans) Iron-containing alcohol dehydrogenases 6614 73 AA848389 G [Caenorhabditis elegans] 21125 74 AA848437 M,L Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with weak similarity to protein sp:Q9WUK2 (M.musculus) IF4H_MOUSE Eukaryotic translation inifiation factor 4H (eIF-4H) (Williams-Beuren symdrome chromosome region 1 protein 23505 75 AA848496 J homolog) Rattus norvegicus transcribed sequence with weak similarity to protein sp:P43165 (R.norvegicus) CAH5_RAT Carbonic anhydrase VA, mitochondrial 11653 76 AA848689 A,F precursor (Carbonate dehydratase VA) (CA-VA) Rattus norvegicus transcribed sequence with wak similarity to protein 21140 77 AA848738 J ref:NP_035246.1 (M.musculus) phospholipase D3 [Mus musculus] 21165 78 AA848941 K actinin, alpha 1 actinin, alpha 1 21166 78 AA848941 K actinin, alpha 1 actinin, alpha 1 Rattus norvegicus transcribed sequence with weak similarity to protein 2924 79 AA848948 H ref:NP_510258.1 (C.elegans) F18H3.1.p [Caenorhabditis elegans] Rattus norvegicus transcribed sequence with strong similarity to protein ref:NP_)62310.1 (M.musculus) hypothetical protein 0610038L10Rik [Mus 22631 80 aa849030 K musculus] 8888 81 AA849036 N,B guanylate cyclase 1, soluble, alpha 3 guanylate cyclase 1, soluble, alpha 3 Rattus norvegicus transcribed sequence with weak similarity to prolein 19412 82 AA849222 D ref:NP_291082.1 (M.musculus) arkadia [Mus musculus] Rattus norvegicus transcribed sequencw with strong similarity to protein ref:NP_062785.1 (M.musculus) acetyl-Coenzyme A symthetase 1 (AMP forming); acetyl-Coenzyme A synthelase 2 (AMP formig); acetyl-CoA 17339 83 AA849497 M synthetase [Mus musculus] Rattus norvegicus transcribed sequence with weak similarity to protein sp:Q63117 (R.norvegicus) CLK3_RAT Protein kinase CLK3 (CDC-like kinase 6635 84 AA849786 M 3) Rattus norvegicus transcribed sequence with strong similarity to protein 18447 85 AA849939 F pdb:1BGM (E. coli) O Chain O, Beta-Galactosidase (Chains I-P) Table 1 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Title Rattus norvegicus transcribed sequence with moderate similarity to protein ref:NP_291042.1 (M.musculus) Mpv17 transgene, kidney disease multant-like 12129 86 AA849966 A,D [Mus musculus] 21341 87 AA850195 I Rattus norvegicus transcribed sequences 14410 88 AA850292 F Rattus norvegicus transcribed sequences 13615 89 AA850364 L Rattus norvegicus transcribed sequences 21766 90 AA850916 J Rattus norvegicus transcribed sequences 1867 91 AA850940 N ribosomal protein L4 ribosomal prolein L4 Rattus norvegicus transcribved sequence with moderate similarity to protein ref:NP_038854.1 (M.musculus) molybdenum cofactor synthesis 2 [Mus 3925 92 AA851017 A,E musculus] 18751 93 AA851169 G protease (prosome,macropain) 28 subunit, beta protease (prosome, macropain) 28 subunit, beta 17823 94 AA851214 D Rattus norvegicus Ba1-643 mRNA, complete cds Rattus norvegicus trnascribed sequencw with moderate similarity to protein 21462 95 AA851261 M,J, ref:NP_054871.1 (H.sapiens) ART-4 protein [Homo sapiens] 13349 96 AA851417 M,H,IU Rattus norvegicus transcribed sequences 1685 97 AA851497 J hemoglobin, alpha 1 hemoglohin, alpha 1 21509 98 AA851618 G epithelial membrane protein 3 epithelial membrane protein 3 splicin factor, arginine/serine-rich (transformer 2 23307 99 AA851749 D Drosophila homolog) 10 splicing factor, arginine/serine-rich (transformes 2 Drosophila homolog) 10 18001 100 AA858573 M spp-24 precursor spp-24 precursor 24377 101 AA858590 H Rattus norvegicus transcribed sequences 17411 102 AA858621 N CaM-kinase II inhibitor alpha CaM-kinase II inhibitor alpha Rattus norvegicus transcribed sequence with strong similarity to protein ref:NP_032594.1 (M.musculus) minichromosome maintenance deficient 7 (S. 1801 1034 AA858636 E cerevisiae) [Mus musculus] 12700 104 AA858673 N pancreatic secretory trypsin inhibitor type II (PTI-II) pancreatic secretory trypsin inhibitor type II (PSTI-II) 18350 105 AA858674 C Rattus norvegicus transcribed sequences Rattus norvegicus trnascribed sequence with weak similarity to protein ref:NP_497482.1 (C.elegans) F53A3.7.p [Caenorhabditis elegans] 7279 107 AA858892 M Rattus norevegicus transcribed sequences Table 1 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Title Rattus norvegicus transcribed sequence with weak similarity to protein sp:P15178 (R.norvegicus) SYD_RAT ASPARTYL-TRNA SYNTHETASE 5867 108 aA858953 M (ASPARTATE-TRANLIGASE) (ASPRS) 6431 109 AA859085 L Rattus norvegicus transcribed sequences 17361 110 AA859114 M,A,G 21025 111 AA859241 M,A,C synaptojanin 2 binding protein synaptojanin 2 binding protein 14124 112 AA859305 N tropomyosin isoform 6 tropomyosin isoform 6 16314 113 AA859348 M,I Rattus norvegicus transcribed sequences Rattus norvegicus trnascribed sequence with strong similarity to protein sp:P07153 (R,norvegicus) RIB1_RAT Dolichyl-diphosphooligosaccharide- 4178 1114 AA859536 M,N,A protein glycosyltransferase 67 kDa subunit precursor (Ribophorin I) (RPN-I) 15150 115 AA859562 N 14353 116 AA859585 D Rattus norvegicus transcribed sequences rattus norvegicus transcribed sequence with moderate similarity to protein pdb:1LBG (E. coli) B Chain B, Lactose Operon Repressor Bound To 21-Base 11852 117 AA859593 N Pair Symmetric Operator Dna, Alpha Carbons Only Rattus norvegicus transcribed sequence with weak similarity to protein 4809 118 AA859616 N ref:NP_502422.1 (C.elegans) FYVE zinc finger [Caenorhabdilis elegans] Rattus norvegicus transcribed sequence with weak similarity to protein 19067 119 AA859663 M,N,B ref:NP_080153.1 (M.musculus) RIKEN cDNA 2310067G05 [Mus musculus] Rattus norvegicus transcribed sequence with weak similarity to protein pdb:1DUB (Rn.norvegicus) F Chain F, 2-Enoyl-Coa Hydratase, Data Collected 20582 120 AA859688 N,A,E,F,K At 100 K, Ph 6.5 Rattus norvegicus transcribed sequence with moderate similarity to protein sp:P51175 (M.musculus) PPOX_MOUSE PROTOPORPHYRINOGEN 14138 121 AA859700 M OXIDASE (PPO) Rattus norvegicus transcribed sequence with weak similarity to protein sp:P20415 (R.norvegicus) IF4E_MOUSE EUKARYOTIC TRANSCLATION INITIATION FACTOR 4E (EIF-4E) (EIF4E) (MRNA CAP-BINDING PROTEIN) 22374 122 AA859804 N (EIF-4F 25 KDA SUBUNIT) Rattus norvegicus transcribed sequence with strong similarity to protein ref:NP_067475.1 (M.musculus) erythoblast macrophage prolein [Mus 11079 123 AA859829 E musculus] Table GLGC GenBank Acc 01 Model ldenlifier Seq ID RelSeq ID Code Known Gene Name UniGene Cluster Title 11481 124 AA859832 B Raltus norvegicus transcnbed sequences 22562 125 AA859835 F Rattus norvegicus transcribed sequences 14184 126 AA859837 M guanine deaminase guanine deaminase 14185 126 AA859837 M guanine deaminase guanine deaminase 22927 127 AA859920 N,E nucleosome assembly protein 1-like 1 nucleosome assembly protein 1-like 1 23000 128 AA859933 F Rattus norvegicus transcribed sequences 23166 129 AA859954 M,C,L vacuole Membrane Protein 1 vacuole Membrane Protein 1 18468 130 AA859966 J Rattus norvegicus transcnbed sequence with moderate similarity to prolein 19377 131 AA859971 A,E ref.NP_079603.1 (M.musculus) RIKEN cDNA 0610010112 [Mus musculus] Rattus norvegicus transcribed sequence with strong similarity to prolein sp:Q9D8N0 (M.musculus) EF1G_MOUSE Elongation factor 1-gamma (EF-1- 4222 132 AA860024 N gamma) (eEF-1B gamma) 13974 133 AA860030 M,F tubulin, beta 5 tubulin, beta 5 7090 134 AA860039 N Rattus norvegicus transcried sequence Rattus norvegicus transcried sequence with strong similarity to prolein 19144 135 AA860049 A pdb: 18GM (E, coli) O Chain O, Beta-Galactosidase (Chains l-P) Rattus norvegicus transcribed sequence with weak similarity to protein sp:P51652 (R.norvegicus) PE2R_RAT 20-alpha-hydroxysteroid 4462 136 AA866264 M,A,C,l dehydrogenase (20-alpha-HSD) (HSD1) 15927 137 AA866321 N Rattus norvegicus transcribed sequences 11865 138 AA866383 N Rattus norvegicus transcribed sequences 9391 139 AA866477 J Rattus norvegicus cytochrome c oxidase subunit Vllb mRNA,complete cds 19402 140 AA874848 N Thymus cell surface antigen Thymus cell surface antigen 18741 141 AA874859 M 16070 142 AA874873 D Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with weak similarity to protein ref:NP_113871.1 (R.norvegicus) segregation of mitotic chromosomes b; SMC 16082 143 AA874887 E (segregation of mitotic chromosomes 1)-like 1 (yeast) [Rattus norvegicus] 16091 144 AA874897 J Rattus norvegicus transcribed sequences 22781 145 AA874926 F Rattus norvegicus focal adhesion kinase (FAK) mRNA, altemative 5'UTR 16139 146 AA874927 N Rattus norvegicus transcribed sequences Table 1 GLGC GenBank Acc or Model ldentifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Title 16312 147 AA875032 M,I,L Rattus norvegicus transcribed sequences 6451 148 AA875033 N fibulin 5 fibulin 5 Rattus norvegicus transoribed sequence with strong similarity to protein sq:P08578 (Mmusculus) RUXE_HUMAN Small nudear ribonucleoprotein E 15419 149 AA875102 N (snRNP-E)(Sm protein E)(Sm-E)(SmE) Rattus norvegicus transcribed sequence with weak similarity to protein ref:NP_032951.1 (M.musculus) protein kinase C substrate BOK-H [Mus 15339 150 AA875171 D musculus] 18084 151 AA875186 N Rattus norvegicus transcribed sequence with strong similanity to protein sp:P55884 (H.sapiens) IF 39_HUMAN Eukaryotic translation initiation factor 3 15371 152 AA875205 N subunit 9 (elF-3 eta) (elF3 p116) (elF3p110) 15376 153 AA875206 N ubiquilin 1 ubiquilin 1 15887 154 AA875225 N GTP-binding protein (G-alpha-i2) GTP-binding protein (G-alpha-i2) 15888 154 AA875225 N GTP-binding protein (G-alpha-i2) GTP-binding protein (G-alpha-i2) 15401 155 AA875257 N Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with strong similarity to protein ref:NP_059128.1 (H.sapiens) prostate tumor over expressed gene 1 [Homo 15421 156 AA875286 C.L sapiens] Rattus norvegicus transcribed sequence with weak similanily to protein ref:NP_072143.1 (R.norvegicus) nucleolin-related protein NRP (NRP) [Rattus 15446 157 AA875327 L norvegicus] 18902 158 AA875390 N thioredoxin-like (32kD) thioredoxin-like (32kD) Rattus norvegicus transcribed sequence with weak similanity to prolein ref:NP_059088.1 (M.musculus) cadherin EGF LAG seven-pass G-type 15505 159 AA875414 N receptor 2 [Mus musculus] 7936 160 AA875496 M,A,B,C,l Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with strong similarity to protein sp:Q64119 (R.norvegicus) MLES_RAT Myosin light chain alkali, smooth- 24472 161 AA875523 L muscle isoform (MLC3SM) 6153 162 AA875531 N Table 1 GLGC GenBank Acc or Model ldentifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Title Rattus norvegicus transcribed sequence with strong similarity to protein ref:NP_084528.1 (M.musculus) hypothetical protein, MGC:7764; hypothetical 15574 163 AA875552 H prolein MGC7764 [Mus musculus] 15295 164 AA875594 M.H.l (FK506 binding protein 2, FK506-binding protein 1a) (FK506 binding prolein 2, FK506-binding protein 1a) 15618 165 AA875620 M Rattus norvegicus transcribed sequences 5384 166 AA891041 l jun B proto-oncogene jun B proto-oncogene 1644 167 AA891068 A.F Peptidylglycine alpha-amidating monooxygenase Peptidylglycine alpha-amidating monooxygenase Rattus norvegicus transcribed sequence with moderale similarity to protein ref:NP_004540.1 (H.sapiens) NADH dehydrogenase (ubiquinone) 1. 15833 168 AA891171 K subcomplex unknow, 2 (14. 5kD, B14.5b) [Homo sapiens] 24235 169 AA891286 M,N,H,l thioredoxin reductase 1 thioredoxin reductase 1 9952 170 AA891422 N hypoxia induced gene 1 hypoxia induced gene 1 Rattus norvegicus transcribed sequence with moderate similarity to prolein 16446 171 AA891423 L ref:NP_078813.1 (H.sapiens) hypothetical prolein FLJ12118 [Homo sapiens] 9071 172 AA891578 N Rattus norvegicus transcribed sequences Rathus norvegicus transcribed sequence with moderate similanity to protein ref:NP_034894.1 (M.musculus) mannosidase 2, alpha B1; lysosomal alpha- 474 173 AA891670 N,D mannosidase [Mus musculus] Rattus norvegicus transcribed sequence with strong similarity to prolein ref:NP_076006.1 (M.musculus) tumor necrosis factor (ligand) superfamily. 9091 174 AA891690 N member 13 [Mus musculus] 17420 175 AA891693 M,N Rattus norvegicus transcribed sequences 18078 176 AA891726 N solute carrier family 34. member 1 solute carrier family 34, member 1 20839 177 AA891729 N ribosomal protein S27a ribosomal protein S27a 11959 178 AA891735 N,D Rattus norvegicus transcribed sequences 17693 179 AA891737 N.J Rathus norvegicus transcribed sequences 14970 180 AA891738 M,B,H,l,K sulfite oxidase sulfite oxidase Rattus norveglcus transcribed sequence with weak similarity to protein 17256 181 AA891739 M,C,E,l ref:NP_496168.1 (C.elegans) F52H3.5.p [Caenorhabdilis elegans] 15110 182 AA891764 M,l low density lipoprotein receptor-related prolein 2 low density lipoprolein receptor-related protein 2 18269 183 AA891769 M,D,L Rattus norvegicus focal adhesion kinase (FAK) mRNA, allernative 5'UTR 9905 184 AA891774 M,A,l,K Rattus norvegious transcribed sequences Table 1 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Title Rattus norvegicus transcribed sequence with weak similarity to protein sp : P41562 (R. norvegicus) IDHC_RAT ISOCITRATE DEHYDROGENASE [NADP] CYTOPLASMIC (OXALOSUCCINATE DECARBOXYLASE) (IDH) 17289 185 AA891785 N, E (NADP+-SPECIFIC ICDH) (IDP) Rattus norvegicus transcribed sequence with weak similarity to protein sp : P41562 (R. norvegicus) IDHC RAT ISOCITRATE DEHYDROGENASE [NADP] CYTOPLASMIC (OXALOSUCCINATE DECARBOXYLASE) (IDH) 17290 185 AA891785 N, E (NADP+-SPECIFIC ICDH) (IDP) Rattus norvegicus transcribed sequence with strong similarity to protein 21672 186 AA891789 C, D ref : NP-062742. 1 (M. musculus) cDNA sequence AB025049 [Mus musculus] 22124 187 AA891790 D Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with moderate similarity to protein 18128 188 AA891800 I ref : NP_008834. 1 (H. sapiens) inorganic pyrophosphatase [Homo sapiens] Rattus norvegicus transcribed sequence with weak similarity to protein sp : P51652 (R. norvegicus) PE2R_RAT 20-alpha-hydroxysteroid 4463 189 AA891831 M, A, I dehydrogenase (20-alpha-HSD) (HSD1) Rattus norvegicus transcribed sequence with weak similarity to protein 20522 190 AA891842 N, L ref : NP057713. 1 (H. sapiens) hypothetical protein LOC51323 [Homo sapiens] Rattus norvegicus transcribed sequence with weak similarity to protein 20523 190 AA891842 N, B, L ref : NP 057713. 1 (H. sapiens) hypothetical protein LOC51323 [Homo sapiens] Rattus norvegicus transcribed sequence with moderate similarity to protein sp : 088338 (M. musculus) CADGMOUSE Cadherin-16 precursor (Kidney- 17249 191 AA891858 N, K specific cadherin) (Ksp-cadherin) Rattus norvegicus transcribed sequence with strong similarity to protein pir : S54876 (M. musculus) S54876 NAD (P) + transhydrogenase (B-specific) (EC 16023 192 AA891872 N 1. 6. 1. 1) precursor-mouse 2576 193 AA891884 K Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with moderate similarity to protein 17779 194 AA891914 N pir : A47488 (H. sapiens) A47488 aminoacylase (EC 3. 5. 1. 14)-human 17933 195 AA891916 K membrane interacting protein of RGS16 membrane interacting protein of RGS16 Table 1 GLGC GenBank Acc or Model ldentifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Title 17438 196 AA891943 M Rattus norvegicus transcribed sequences 1159 197 AA891949 M,N,D,l Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with strong similarity to protein 4473 198 AA891965 M,A,D,l ref:NP_071297.1 (M.musculus) fructosamine 3 kinase [Mus muscus] 17088 199 AA891998 B,L sequestosome 1 sequestosome 1 Rattus norvegicus transcribed sequence with weak similarity to protein sp:P50517 (R.norvegicus) VAB2_MOUSE Vacuolar ATP synthase subunit B, brain isoform (V-ATPase B2 subunity) (Vacuolar prolon pump Bisoform 2)2107 200 AA892006 D,K (Endomembrane proton pump 58 kDa subunit) 17630 201 AA892012 N glutamate oxaloacetate transaminase 2 glutamate oxaloacetate transaminase 2 17345 202 AA892014 E HLA-B-associated transcript 1A HLA-B-associated transcript 1A 23047 203 AA892027 M Rattus norvegicus transcribed sequences 19252 204 AA892041 H peroxiradoxin 6 peroxiredoxin 6 Rattus norvegicus transcribed sequence with weak similarity to protein 13420 205 AA892042 N pir.JC2534 (R.norvegicus) JC2534 RVLG protein - rat Rattus norvegicus transcribed sequence with strong similarity to protein ref:NP_062419.2 (M.musculus) proline dehydrogenase (oxidase) 2, prolin 19469 206 AA892112 M,D oxidase 1; kidney and liver proline oxidase 1 [Mus musculus] 4259 207 AA892123 N ribosomal protein L36 ribosomal protein L36 14595 208 AA892128 N,B,L Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with moderate similarity to protein ref:NP_060937.1 (H.sapiens) uncharacterized hematopoietic stem/progenitor 15576 209 AA892132 J cells protein MDS032 [Homo sapiens] Rattus norvegious transcribed sequence with moderate similarity to prolein pdb:1LBG (E. coli) B Chain B, Lactose Operon Repressor Bound To 21-Base 16529 210 AA892154 N Paire Symmetric Operator Dna, Alpha Carbons Only 4482 211 AA892173 N Rattus norvegicus transcribed sequence Rattus norvegicus transcribed sequence with strong similarity to protein ref:NP_079845.1 (M.musculus) microsomal glutathione S-transferase 3 [Mus 8317 212 AA892234 M,N muscukis] 4484 213 AA892258 N NADPH oxidase 4 NADPH oxidase 4 9073 214 AA892273 J Rattus norvegicus transcribed sequences 18190 215 AA892280 M,N Rattus norvegicus transcribed sequences Table 1 GLGC GenBank Acc or Model ldentifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Title Rattus norvegicus transcribed sequence with weak similarity to protein ref:NP_061123.2 (H.sapiens) G protein-coupled receptor, family C, group 5, member C, isoform b, precursor, orphan G-prolein coupled receptor, retinoic acid inducible gene 3 prolein; retinoic acid responsive gene protein [Homo 17717 216 AA892287 N saplens] Rattus norvegicus transcribed sequence with strong similarity to protein 4373 217 AA892310 F ref:NP_080731.1 (M.musculus) RIKEN cDNA 2510049119 [Mus musculus] potassium inwardly-rectifying channel, subfamily J. 9027 218 AA892312 N member 16 potassium inwardly-rectifying channel, subfamily J, member 16 17161 219 AA892333 M alpha-tubulin alpha-tubulin 17684 220 AA892345 M,# dimethylglycine dehydrogenase precursor dimethylglycine dehydrogenase precursor Rattus norvegicus transonbed sequence with strong similarity to prolein 13647 221 AA892367 N,G sp:P21531 (R.norvegicus) RL3_RAT 60S RIBOSOMAL PROTEIN L3 (L4) 19768 222 AA892373 M,C,G synlenin synlenin Rattus norvegicus transcribed sequence with strong similarity to protein 3474 223 AA892378 C ref:NP_079838.1 (M.musculus) RIKEN cDNA 2010003O14 [Mus musculus] 17682 224 AA892382 M,l camello-like 1 camello-like 1 (Rattus norvegicus transcribed sequence with strong similarity to protein sp:P00884 (R.norvegicus) ALFB_RAT FRUCTOSE-BISPHOSPHATE 820 225 AA892395 N aldolase B ALDOLASE B (LIVER-TYPE ALDOLASE), aldolase B) 12016 226 AA892404 N,C Na+ dependent glucose transporter 1 Na+ dependent glucose transporter 1 23194 227 AA892417 M ephrin A1 ephrin A1 Rattus norvegicus transcribed sequence with strong similarity to protein 16469 228 AA892462 A,C ref:NP_079926.1 (M.musculus) RIKEN cDNA 0710008D09 [Mus musculus] 13609 229 AA892468 M,H,l prolease, serine, 8 (prostasin) protease, serine, 8 (prostasin) M,A,C,F,H, 13610 229 AA892468 l,K protease, serine, 8 (prostasin) protease, serine, 8 (prostasin) 11901 230 AA892483 B Rattus norvegicus transcribed sequences 21695 231 AA892506 N,G coronin, actin binding protein 1A coronin, actin binding protein 1A Rattus norvegicus transcribed sequence with weak similarity to protein ref:NP_077053.1 (R.norvegicus) calcium binding protein P22 [Rattus 4499 232 AA892511 N norvegicus] 8599 233 AA892522 M,N,F Rattus norvegicus transcribed sequences Table 1 GLGC GenBank Acc or Model ldentifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Title 15154 234 AA892532 N prolein disulfide isomerase-related protein protein disulfide isomerase-related protein 12275 235 AA892541 N Rattus norvegicus transcribed sequences 12276 235 AA892541 M,N,D,L Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with moderate similarity to protein ref:NP_032793.1 (M.musculus) organic cationic transporter-like 2 [Mus 17468 236 AA892545 D musculus] 17469 237 AA892549 D Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with moderate similarity to prolein 18906 238 AA892561 M,l ref:NP_054758.1 (H.sapiens) PTD012 protein [Homo sapiens] Rattus norvegicus transcribed sequence with strong similarity to prolein 18274 239 AA892572 N ref:NP_079639.1 (M.musculus) RIKEN cDNA 1110001J03 [Mus musculus] Rattus norvegicus transcribed sequence with strong similarity to protein 18275 239 AA892572 N,K ref.NP_079639.1 (M.musculus) RIKEN cDNA 1110001J03 (Mus msculus] Rattus norvegicus transcribed sequence with strong similarity to protein 4512 240 AA892578 N ref:NP_116238.1 (H.sapiens) hypothetical protein FLJ14834 [Homo saplens] 15876 241 AA892582 N,G aldehyde dehydrogenase family 3, member A1 aldehyde dehydrogenase family 3, member A1 19085 242 AA892598 M nucleostemin nucleostemin 19086 242 aA892598 M nucleostemin nucleostemin solute carrier family 13 (sodium-dependent solute carrier family 13 (sodium-dependent dicarboxylate transporter), 17500 243 AA892616 N dicarboxylate transporter), member 3 member 3 20088 244 AA892666 K Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with moder ate similarity to protein pdb:1LBG (E. coli) B Chain B, Lactose Operon Repressor Bound To 21-Base 23783 245 AA892773 M,N,l,K Pair Symmetric Operator Dna. Alpha Carbons Only 19251 246 AA892796 C Rattus norvegicus transcribed sequences 13542 247 AA892798 N,B ulerine sensitization-associated gene 1 protein utenne sensilization-assoclated gene 1 protein Rattus norvegicus transcnbed sequence with weak similarity to protein ref:NP_113808.1 (R.norvegicus) 3-phosphoglycerate dehydrogenase [Rattus 22537 248 AA892799 M,A,D norvegicus] Rattus norvegicus transcribed sequence with weak similarity to protein ref:NP_113808.1 (R.norvegicus) 3-phosphoglycerate dehydrogenase [Rattus 22538 248 AA892799 M,D norvegicus] Table 1 GenBank Acc or Model Identifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Title Rattus norvegicus transcribed sequence with weak similarity to protein ref : NP_113808. 1 (R. norvegicus) 3-phosphoglycerate dehydrogenase [Rattus 22539 248AA892799 M, N norvegicus] 15385 249 AA892808 N isocitrate dehydrogenase 3, gamma isocitrate dehydrogenase 3, gamma low density lipoprotein receptor-related protein 408 250 M892810 M associated protein 1 low density lipoprotein receptor-related protein associated protein 1 Rattus norvegicus transcribed sequence with weak similarity to protein 4529 251 AA892818 M pir : S54293 (R. norvegicus) S54293 regulator protein p122-RhoGAP-rat aldo-keto reductase family 7, member A2 (aflatoxin 23321 252 CA892821 M aldehyde reductase) aldo-keto reductase family 7, member A2 (aflatoxin aldehyde reductase) aldo-keto reductase family 7, member A2 (aflatoxin 23322 252 M892821 N aldehyde reductase) aldo-keto reductase family 7, member A2 (aflatoxin aldehyde reductase) Rattus norvegicus transcribed sequence with strong similarity to protein prf : 2204316A (M. musculus) 2204316A ATP sulfurylase-adenosine 17332 253 AA892829 J phosphosulfate kinase [Mus musculus] Rattus norvegicus transcribed sequence with moderate similarity to protein 17923 254 AA892843 D ref : NP078816. 1 (H. sapiens) hypothetical protein FLJ20917 [Homo sapiens] Rattus norvegicus transcribed sequence with strong similarity to protein pir : S25716 (M. musculus) S25716 Ras guanine nucleotide exchange factor 18887 255 AA892860 J son-of-sevenless (sos) 1-mouse 3053 256 M892861 Rattus norvegicus transcribed sequences 12848 257 M892916 N, H K Rattus norvegicus Ab2-305 mRNA, complete cds 3438 258 AA892921 K Rat mRNA fragment with B2 repetitive sequence (clone pAR24) Rattus norvegicus transcribed sequence with moderate similarity to protein pdb : 1 G51 (M. musculus) A Chain A, Crystal Structure Of The Accessory 14465 259 AA892950 K Subunit Of Murine Mitochondrial Polymerase Gamma 3853 260 AA892999 N, K Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with strong similarity to protein pir : T00335 (H. sapiens) T00335 hypothetical protein KIAA0564-human 3439 261 AA893000 N, B (fragment) 12020 262 AA893035 N HP33 HP33 3863 263 M893060 C, D Rattus norvegicus transcribed sequences Table 1 GLGC GenBank Acc or Model ldentifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Title 13332 264 AA893080 M,K Rattus norvegicus transisoribed sequences 21305 265 AA893082 M,D,H,l Rattus norvegious transcribed sequences 3870 266 AA893147 N,F,G Rattus norvegicus transcribed sequences Ratlus norvegicus transcribed sequence with moderate simllarity to protein ref.NP_002483.1 (H.sapiens) NADH dehydrogenase (ubiquinone) 1 beta 16881 267 AA893185 J subcomplex, 5 (15kD, SGDH) [Homo sapiens] 17447 268 AA893192 M Rattus norvegicus transcribed sequences Rattus norvegices transcribed sequence with weak similarity to prolein ref:NP_062289.1 (M.musculus) nuclear localization signals binding prolein 1 17744 269 AA893206 M [Mus musculus] Rattus norvegicus transcribed sequence with weak similarity to protein sp:Q61585 (M.musculus) G0S2_MOUSE Putaive lymphocyle G0/G1 switch 548 271 AA893235 N protein 2 (G0S2-like protein) 17752 272 AA893244 N Rattus norvegicus transcribed sequerices Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with weak similarityto protein 18967 273 AA893260 N,H ref:NP_083358.1 (M.musculus) RIKEN cDNA 5830411J07 [Mus musculus] Rattus norvegicus transcribed sequence with weak similarity to protein sp:P43884 (R.norvegicus) PLIN_RAT Perilipin (PERl)(Lipid droplet- 16168 274 AA893280 M,J associated protein) Rattus norvegicus transcribed sequence with moderate similarity to protein pdb:1LBG (E. coli) B Chain B, Laclose Operon Repressor Bound To 21-Base 3886 275 AA893289 J Pair Symmetric Operator Dna, Alpha Carbons Only 4242 276 aA893325 N omithine aminotransferase omithine aminotransferase 9082 277 AA893357 M Rattus norvegicus transcribed sequences 17800 278 AA893436 K Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with moderate similarity to protein sp:O09015 (R.norvegicus) MXl1_RAT MAX interacting protein 1 (MX11 3465 279 AA893611 M,B,F protein) Rattus norvegicus transcribed sequence with weak similanily to protein ref:NP_112249.1 (R.norvegicus) guanine nucleotide-binding protein, beta-1# 17836 280 AA893626 D subunit [Rattus norvegicus] Table 1 GLGC GenBank Acc or Model ldentifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Title Rattus norvegicus transcribed sequence with weak simitarity to protein ref:NP_113981.1 (R.norvegicus) matrin cyclophilin (matrin-cyp) [Rattus 4542 281 AA893643 C norvegicus] 7505 282 AA893702 N,A transcobalarrin ll precursor transcobalamin ll precursor Rattus norvegicus transcribed sequence with strong similarity to protein ref:NP_036155.1 (M.musculus) Rac GTPase-activating protein 1 [Mus 9084 283 AA893717 N,E musculus] Rattus norvegicus transcribed sequence with strong similarity to prolein ref:NP_149065.1 (M.musculus) hypothetical protein D15Wsu59e [Mus 12031 284 AA893860 M,l musculus] Rattus norvegicus transcribed sequence with moderale similanty to protein ref.NP_446379.1 (R.norvegicus erythrocyte protein band 4.1-like 3 [Rattus 2128 285 AA894008 B norvegicus] 10540 286 AA894027 N 3895 287 AA894029 N Rattus norvegicus transcribed sequences 2191 288 AA894086 F Rattus norvegicus Ac1133 mRNA. complete cds 2979 289 AA894099 H vacuolar protein sorting prolein 4a vacuolar protein surting prolein 4a Rattus norvegicus transonibed sequence with strong similarity to protain pir:A31568 (R.norvegicus) A31568 electron transfer flavoprolein alpha chain 16435 290 AA894174 N precursor-rat 22783 291 AA894207 A.F Rattus norvegicus focal aclhesion kinase (FAK) mRNA, allemative 5'UTR 16849 292 AA894298 N membrane metallo endopeptidase membrane metallo endopeptidase 21587 293 AA899141 D 3-phosphoglycerate dehydrogenase 3-phosphoglycerate dehydroenase 24329 294 AA899253 N myristoylated alanine rich protein kinase C substrate myrisloylated alanine rich protein kinase C substrate Rattus norvegicus transcribed sequence with strong similarity to protein 22490 295 AA899289 A ref:NP_055787.1 (H.sapiens) KiAA1049 protein (Homo sapiens] 4661 296 AA899709 M,B,L receptor (calcitonin) activity modifying protein 3 receptor (calcitonin) activity modifying protein 3 21354 297 AA899721 B,L Rattus norvegicus transcribed sequences 23778 298 AA899854 N,E topoisomerase (DNA) 2 alpha topoisomerase (DNA) 2 alpha 9114 299 AA899951 M Rattus norvegicus transcribed sequences 9541 300 AA900505 N,L rhoB gene rhoB gene Table 1 GLGC GenBank Acc or Model ldentifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Title Rattus norvegicus transcribed sequence with weak similarity to protein sp:Q63413 (R.norvegicus) HE47_RAT Probable ATP-dependent RNA 3822 301 AA900863 M,H helicase p47 Rattus norvegicus transcribed sequence with weak similarity to protein 3959 302 AA901338 M pir.A47305 (R.norvegicus) A47305 transtation initiation factor elF-5-rat 12355 303 AA923857 D Carcinoembryonic antigen gene family (CGM3) Carcinoembryonic antigen gene family (CGM3) Rattus norvegicus transcribed sequence with moderate similarity to protein ref.NP_034081.1 (M.musculus) insulin-like growth factor 2, binding protein 1; coding region determinant binding protein; zipcode-binding protein 1; zipcode 6736 304 AA924005 C binding protein 1 [Mus musculus] 17477 305 AA924029 M,K,L phospholipid scramblase 1 phospholipid scramblase 1 24192 306 AA924210 H 3-hydroxy-3-methylglutaryl-Coenzyme A reductase 3-hydroxy-3-methylglutaryl-Coenzyme A reductase 20711 307 AA924267 N,L cytochrome P450,4A1 cytochrome P450,4A1 4933 308 AA924301 M,A Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with strong similarity to protein 23093 309 AA924342 G ref:NP_064571.1 (H.sapiens) DC11 protein [Homo sapiens] Rattus norvegicus transcribed sequence with weak similarity to protein ref:NP_068522.1 (R.norvegicus) Nopp140 associated protein [Rattus 4944 310 AA924405 M,H,l,K norvegicus] Rattus norvegicus transcribed sequence with weak similarity to prolein sp:Q9JH17 (M.musculus) PMC1_MOUSE Polymyositis/scleroderma autoanligen 1 (Autoantigen PM/Scl 1) (Polymyositis/scleroderma autoantigen 75 kDa) (PM/Scl-75)(P75 polymyositis-scleroderma overlap syndrome 3631 311 AA924460 D associated autoanfigen) Rattus norvegicus transcribed sequence with strong similarity to protein pir:T12449 (H.sapiens) T12449 hypothetical protein DKFZp564E1616.1- 22984 312 AA924560 E human (fragments) Rattus norvegicus transcribed sequence with weak similarity to prolein ref:NP_113808.1 (R.norvegicus) 3-phosphoglycerate dehydrogenase [Rattus 22540 313 AA924630 E norvegicus] Table 1 GLGC GenBank Acc or Model ldentifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Title Rattus norvegicus transcribed sequence with weak similarity to pretein sp:Q9Z1P2 (R.norvegicus) AAC1_RAT Alpha-actinin 1 (Alpha-actinin cytoskeletal isoform) (Non-muscle alpha-actinin 1) (F-actin cross linking 23123 314 AA924794 K protein) Rattus norvegicus transcribed sequence with weak similarity to prolein sp:P27435 (R.norvegicus) MCT7_RAT Mast cell protease 7 precursor (RMCP- 23195 315 AA925026 M 7) (Tryptase.skin) Rattus norvegicus transcribed sequence with strong similarity to protein 21458 316 AA925049 M pdb:1BGM (E. coli) O Chain O. Beta-Galactosidase (Chains l-P) 14790 317 AA925087 M Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with weak similarity to protein ref:NP_110477.1 (R.norvegicus) betaine-homocysteine methyltransferase 23261 318 AA925145 M,l [Rattus norvegicus] Rattus norvegicus transcribed sequence with weak similarity to protein prf:2118320A (R.norvegicus) 2118320A neurodegeneration-associated 17363 319 AA925150 F,K protein 1 [Rattus norvegicus] Rattus norvegicus transcribed sequence with moderate similarity to protein 18271 320 AA925267 M,l ref:NP_055993.1 (H.sapiens) KlAA0717 protein [Homo sapiens] 5129 321 AA925335 J Rattus norvegicus transcribed sequences 23978 322 AA925352 M,L Rattus norvegicus transcribed sequences 22479 323 AA925418 B,L Rattus norvegicus transcribed sequences succinate dehydrogenase complex, subunit A, 17514 324 AA925554 E,G flavoprotein (Fp) succinate dehydrogenase complexx, subunit A, flavoprotein (Fp) Rattus norvegicus transcribed sequence with weak similarity to protein sp:Q9JK41 (R.norvegicus) COP1_RAT High-affinity copper uptake protein 1 5183 325 AA925662 L (rCTR1)(Copper transporter 1) 5205 326 AA925747 K Rattus norvegicus transcribed sequences 5206 327 AA925755 E glutaminase glutaminase Rattus norvegicus transcribed sequence with moderate similarity to protein ref:NP_444278.1 (H sapiens) mitochondrial ribosomal protein L53 (Homo 20866 328 AA926098 J sapiens] Rattus norvegicus transcribed sequence with strong similarity to protein 17157 329 AA926129 M,N ref:NP_446139.1 (R.norvegicus) schlafen 4 [Rattus norvegicus] Table 1 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Title Rattus norvegicus transcrited sequence with strong similarity to protein 16468 330 AA926137 N.A ref:NP_079926.1 (M.musculus) RIKEN cDNA 0710008D09 [Mus musculus] 13411 331 AA926196 M Rattus norvegicus transcribed sequences 5295 332 AA926247 M,L putative potassium channel TWIK putative potassium channel TWIK 21513 333 AA926261 H Rattus norvegicus transcribed sequences 22928 334 AA926262 M neuronal regeneration related protein neuronal regeneration related protein 894 335 AA926305 E Rattus norvegicus transcribed sequences 15028 336 Aa942685 N,F cytosolic cysteine dioxygenase 1 cytosolic cysteine dioxygenase 1 6039 337 AA942716 M,G Rattus norvegicus HN1 mRNA, complete cds 23005 338 AA942770 1 Rattus norvegicus transcribed sequences 21318 339 AA942774 M Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with weak similarity to protein 18168 340 AA942995 E pir:T14346 (M.musculus) T14346 herc2 protein - mouse Rattus norvegicus transcribed sequence with strong similarity to protein pir:S16385 (R norvegicus) S16385 macrophage colony-stimulating factor 1 6691 341 AA943028 J receptor precusor - rat Rattus norvegicus transcribed sequence with strong similarity to protein ref:NP_445869.1 (R.norvegicus) GRB2-associated binding protein 2 [Rattus 22180 342 AA943202 D norvegicus] 21990 343 AA943524 C Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with moderate similarity to protein sp:P43406 (M. musculus) ITAV_MOUSE Integrin alpha-V precursor 12673 344 AA943773 D,L (Vitronectin receptor alpha subunit) (CD51) 18285 345 AA943791 F Rattus norvegicus transcribed sequences 21696 346 AA944324 N,C ADP-ribosylation factor 6 ADP-ribosylation factor 6 22681 347 AA944413 M,I Rattus norvegicus transcribed sequence with strong similarity ot protein sp:Q9JHN8 (M muscutus) ST19_MOUSE Serine/threonine-protein kinase 19 6711 348 AA944439 M (RP1 protein) Rattus norvegicus transcribed sequence with weak similarity to protein sp:P57756 (R.norvegicus) FCN2_RAT Ficolin 2 precursor (Collagen/fibrinogen domain-containing protein 2) (Ficolin-B) (Ficolin B) (Serum lectin P35) (EBP- 14763 349 AA944481 L 37) (Hucolin) Table 1 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Title 22536 350 AA944803 K R norvegicus mRNA for parathyroid hormone regulated sequence (202bp) 22501 351 AA944811 H putative zinc finger protein SERZ-1 putative zinc finger protein SERZ-1 11974 352 AA944958 M R.norvegicus mRNA for 3'UTR of CDK6 (unknown) protein 22554 353 AA945076 M,I glycerol kinase glycerol kinase 1798 354 AA945569 M,D pregnancy-zone protein pregnancy-zone protein 15175 355 AA945583 E hydroxysteroid (17-beta) dehydrogenase 10 hydroxysteroid (17-beta) dehydrogenase 10 20812 356 AA945611 N ribosomal protein L10 ribosomal protein L10 Rattus norvegicus transcribed sequence with weak similarity to protein pir A34162 (R nouvegicus) A34162 NAD(P)H dehydrogenase (quinone) (EC 22612 357 AA945624 M,I 1.6.99.2) - rat 22618 358 AA945656 E Rattus norvegicus transcribed sequences 22625 359 AA945704 H Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with strang similarity to protein ref:NP_064624.1 (H.sapiens) small protein effector 1 of Cdc42 [Homo 22656 360 AA945818 M,H sapiens] 22351 361 AA945867 N v-jun sarcoma virus 17 oncogene homolog (avian) v-jun sarcoma virus 17 oncogene homolog (avian) 5565 362 AA945879 M,C Bardet-Biedl syndrome 2 (human) Bardet-Biedl syndrome 2 (human) 21976 363 AA946011 B Rattus norvegicus transcribed sequences 18524 364 AA946017 D Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with strong similarity to protein 20832 365 Aa946040 A ref:NP_079904.1 (M.musculus) RIKEN cDNA 2010000G05 [Mus musculus] 18337 366 AA946046 M,I Rattus norvegicus transcribed sequences 826 367 AA946108 M,A laminin 5 alpha 3 laminin 5 alpha 3 Rattus norvegicus transcribed sequence with strong similarity to protein 21157 368 AA946189 I pir:A36983 (M musculus) A36983 RNA1 homolog fug1-mouse 22770 369 AA946428 D Rattus norvegicus transcribed sequences X-prolyl aminopeptidase (aminopeptidase P) 2, 12331 370 AA946466 M,H membrane-bound X-prolyl aminopeptidase (aminopeptidase P) 2, membrane-bound X-prolyl aminopeptidase (aminopeptidase P) 2, 12332 370 AA946466 M,G membrane-bound X-prolyl aminopeptidase (aminopeptidase P) 2, membrane-bound 17499 371 AA946467 M Rattus norvegicus transcribed sequences 1809 372 AA946503 G,K lipocalin 2 lipocalin 2 9452 373 AA955206 M fibrinogen-like 2 fibrinogen-like 2 Table 1 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Title 23512 374 AA955282 M Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with weak similarity to protein ref:NP_072143.1 (R.norvegicus) nucleolin-related protein NRP (NRP) [Rattus 22596 375 AA955298 M norvegicus] 19347 376 AA955334 D 23532 377 AA955347 E 23533 378 AA955350 E Rattus norvegicus transcribed sequences 23546 379 AA955393 I Rattus norvegicus transcribed sequences 23626 380 AA955540 D Rattus norvegicus transcribed sequences 23718 381 AA955790 A unr protein unr protein 498 382 AA956278 M Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with weak similarity to protein pir B34252 (R.norvegicus) B34252 acyl-CoA dehydrogenase (EC 1.3.99.3) 23758 383 AA956414 C,G short-chain-specific precursor, hepatic-rat Rattus norvegicus transcribed sequence with strang similarity to protein 23790 384 AA956499 D ref:NP_060640.1 (H.sapiens) hypothetical protein FLJ10656 [Homo sapiens] 19936 385 AA956517 D ceroid-lipofuscinosis, neuronal 2 ceroid-lipofuscinosis, neuronal 2 23834 386 Aa956659 C Rattus norvegicus transcribed sequences 23839 387 AA956684 D Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with moderate similarity to protein pir:JC4761 (M.musculus) JC4761 recombination activating gene 1 inducing 18288 388 AA956813 C protein-mouse Rattus norvegicus transcribed sequence withy weak similarity to protein ref:NP_113997.1 (R.norvegicus) cyclic nucleotide-gated channel beta suburit 5990 389 AA956907 M 1 [Rattus norvegicus] Rattus norvegicus transcribed sequence with moderate similarity to protein 23957 390 AA957123 M ref:NP_033879.1 (M.musculus) brain expressed X-lined 2 [Mus musculus] 23958 391 AA957125 E Rattus norvegicus transcribed sequences 16731 392 AA957244 D tumor necrosis factor receptor superfamily, member 23314 393 AA957270 H,I 12a tumor necrosis factor receptor superfamily, member 12a Table 1 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Title Rattus norvegicus transcribed sequence with strong similarity to protein sp : P26638 (M. musculus) SYS_MOUSE Seryl-tRNA synthetase (Serine--tRN} 2702 394 AA957307 M, I, J ligase) (SerRS) 23843 395 M957410 D Rattus norvegicus transcribed sequences 24051 396 M957452 J Rattus norvegicus transcribed sequence 17523 397 AA963240 D Rattus norvegicus transcribed sequences 24246 398 AA963703 H 2195 399 M963746 M Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with weak similarity to protein sp : Q09167 (R. norvegicus) SFR5_RAT Splicing factor, arginine/serine-rich 5 (Pre-mRNA splicing factor SRP40) (Insulin-induced growth response protein 9309 400 AA963794 E CL-4) (Delayed-early protein HRS) 2232 401 AA963990 D Rattus norvegicus transcribed sequences 2282 402 AA964147 F Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with weak similarity to protein ref : NP079792. 1 (M. musculus) serologically defined breast cancer antigen 2113 403 AA964275 D 84 [Mus musculus] 2423 404 AA964611 D Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with weak similarity to protein sp : P97852 (R. norvegicus) DHB4_RAT Estradiol 17 beta-dehydrogenase 4 (17 2457 405 AA964752 L beta-HSD 4) (17-beta-hydroxysteroid dehydrogenase 4) (HSD IV) 24233 406 AA964756 F centrin 2 centrin 2 12561 407 AA964815 M, C Rattus norvegicus transcribed sequences 11324 408 AA964832 J, L 21339 409 AA964962 J, L ATP-binding cassette, sub-family A (ABC1), member 1 ATP-binding cassette, sub-family A (ABC1), member 1 Rattus norvegicus transcribed sequence with strong similarity to protein 2563 410 AA965113 K ref : NP_080588. 1 (M. musculus) RIKEN cDNA 2610029G23 [Mus musculus] Rattus norvegicus transcribed sequence with strong similarity to protein ref : NP035433. 1 (M. musculus) retinal short-chain dehydrogenase/reductase 2569 411AA965122 K1 [Mus muscuius] 645 412 AA965132 G, K solute carrier family 12, member 3 solute carrier family 12, member 3 2905 413 AA996727 M Rattus norvegicus transcribed sequences Table 1 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Title 2964 414 AA996954 F Rattus norvegicus transcribed sequences 20694 415 AA997048 M,I Rattus norvegicus transcribed sequences 3145 416 AA997237 D Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with strong similarity to protein sp:P48004 (R.norvegicus) PSA7_RAT Proteasome subunit alpha type 7 3172 417 AA997406 B (Proteasome subunit RC6-1) 12616 418 AA997599 E Rattus norvegicus transcribed sequences 3020 419 AA997656 L Rattus novegicus transcribed sequences Rattus norvegicus transcribed sequence with strong similarity to protein 3053 420 AA997726 H sp:Q14690 (H.sapiens) RRP5_HUMAN RRP5 protein homolog (Fragment) Rattus norvegicus transcribed sequence with moderate similarity to protein 3269 421 AA997800 E pir:T30249 (M.musculus) T30249 cell proliferation antigen Ki-67 - mouse 20035 422 AA997933 M,H Nopp140 associated protein Nopp140 associated protein 3407 423 AA997953 F TCF3 (E2A) fusion partner (in childhood leukemia) TCF3 (E2A) fusion partner (in childhood leukemia) 21959 424 AA997973 D,E core binding factor beta core binding factor beta Rattus norvegicus transcribed sequence with weak similarity to protein ref:NP_034202.1 (M.musculus) dolichol-phosphate (beta-D) 16625 425 AA998062 D mannosyltransferase 1 [Mus musculus] Rattus norvegicus transcribed sequence with weak similarity to protein 3572 426 AA998516 E sp:P30277 (R.norvegicus) CGB1_RAT G2/mitotic-specific cyclin B1 2782 427 AA998565 J cyclin-dependent kinase inhibitor 1C, p57 cyclin-dependent kinase inhibitor 1C, p57 Rattus norvegicus transcribed sequence with weak similarity to protein ref:NP_446222.1 (R.norvegicus) Arg/Abl-interacting protein ArgBP2 [Rattus 22737 428 AA998660 L norvegicus] 17734 429 AA998683 M,C,I heat shock 27kDa protein 1 heat shock 27kDa protein 1 Rattus norvegicus transcribed sequence with strong similarity to protein 11558 430 AA998894 D ref:NP_079615.1 (M. musculus) RIKEN cDNA 0610027O18 [Mus musculus] Rattus norvegicus transcribed sequence with strong similarity to protein ref:NP_109674.1 (M.musculus) endoplasmic reticulum chaperone SIL 1 3069 431 AA998910 G homolog (S. cerevisiae) [Mus musculus] 3079 432 AA999169 M 21211 433 AB000098 C MIPP65 protein MIPP65 protein 1962 434 AB000199 J CCA2 protein CCA2 protein Table 1 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Title 1509 435 AB000507 N,A aquaporin 7 aquaporin 7 17337 436 AB000717 N 1535 437 AB000778 F phospholipase D gene 1 phospholipase D gene 1 1382 438 AB002406 G ruvB-like protein 1 ruvB-like protein 1 7914 439 AB002584 N beta-alanine-pyruvate aminotransferase beta-alanine-pyruvale aminotransferase solute carrier family 22 (organic anion transporter), 1510 440 AB004559 M,D,K member 6 solute carrier family 22 (organic anion transporter), member 6 20708 441 AB006461 A neurochondrin neurochondrin 3512 442 AB006607 F choline/ethanolamine kinase choline/ethanolamine kinase 15750 443 AB007690 H homer, neuronal immediate early gene, 2 homer, neuronal mmediate early gene, 2 15703 444 AB009372 N lysophospholipase lysophospholipase 15662 445 AB010119 N,G t-complex testis expressed 1 t-complex testis expressed 1 1857 446 AB010428 L cytosolic acyl-CoA thioesterase 1 cytosolic acyl-CoA thioesterase 1 ATP-binding cassette, sub-family C (CFTR/MRP), 15701 447 AB010467 A,I member 3 ATP-binding cassette, sub-family C (CFTR/MRP), member 3 4312 448 AB010635 N,J carboxylesterase 2 (intestine, liver) carboxylesterase 2 (intestine, liver) 13973 449 AB011679 N,E tubulin, beta 5 tubulin, beta 5 1422 450 AB012759 M,B,G,L prolyl endopeptidase prolyl endopeptidase 15926 451 AB012933 D fatty acid Coenzyme A ligase, long chain 5 fatty acid Coenzyme A ligase, long chain 5 20457 452 AB012944 M,B,K,L parathyroid hormone receptor parathyroid hormone receptor 18300 453 AB013453 M,H,I,L Rattus norvegicus mRNA for NaPi-2 alpha, complete cds 18075 454 AB013455 N solute carrier family 34, member 1 solute carrier family 34, member 1 18076 454 AB013455 N solute carrier family 34, member 1 solute carrier family 34, member 1 18597 455 AB013732 N,B,H UDP-glucose dehydrogeanse UDP-glucose dehydrogeanse 2632 456 AB016489 A,D jumping translocation breakpoint jumping translocation breakpoint (argininosuccinate lyase, heterogeneous nuclear 4234 457 AB016536 N,K ribonucleoprotein A/B) (argininosuccinate lyase, heterogeneous nuclear ribonucleoprotein A/B) 23625 458 AB017260 N,D solute carrier family 22, member 5 solute carrier family 22, member 5 15242 459 AB017912 D MAD homolog 2 (Drosophila) MAD homolog 2 (Drosophila) 15243 459 AB017912 N MAD homolog 2 (Drosophila) MAD homolog 2 (Drosophila) 954 460 AF000114 B contactin associated protein 1 contactin associated protein 1 1727 461 AF001417 M core promoter element binding protein core promoter element binding protein 18070 462 AF003008 M,N max interacting protein 1 max interacting protein 1 Table 1 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Title 1511 463 AF004017 D solute carrier family 4, member 4 solute carrier family 4, member 4 7488 464 AF007758 N synuclein, alpha synuclein, alpha 7489 464 AF007758 M,G,I,J,L synuclein, alpha synuclein, alpha 1183 465 AF013144 N MAP-kinase phosphatase (cpg21) MAP-kinase phosphalase (cpg21) 1081 466 AF013145 M,D PDZ domain containing 1 PDZ domain containing 1 19254 467 AF014009 H peroxiredoxin 6 peroxiredoxin 6 1597 468 AF014503 L nuclear protein 1 nuclear protein 1 18074 469 AF015305 K solute carrier family 29, member 2 solute carrier family 29, member 2 1483 470 AF020618 M,I myeloid differentiation primary response gene 116 myeloid differentiation primary response gene 116 18043 470 AF020618 F myeloid differentiation primary response gene 116 myeloid differentiation primary response gene 116 16407 471 AF022247 N cubilin cubilin 19665 472 AF022819 D,L putative potassium channel TWIK putative potassium channel TWIK 25165 473 AF022952 N vascular endothelial growth factor B vascular endothelial growth factor B 23868 474 AF023087 M,L early growth response 1 early growth response 1 16116 475 AF025670 F caspase 6 caspase 6 25168 476 AF030050 A replication factor C replication factor C 3454 477 AF030091 N,J cyclin L cyclin L 15790 478 AF032120 E regulator of G-protein signaling 19 interacting protein 1 regulator of G-protein signaling 19 interacting protein 1 2439 479 AF032668 A,F SEC15 homolog (S. cerevisiae) SEC15 homolog (S. Cerevisiae) 23045 480 AF034218 N hyaluronidase 2 hyaluronidase 2 15800 481 AF035822 A synaptosomal-associated protein, 29kD synaptosomal-associated protein, 29kD 1564 482 AF035963 E,G,K kidney injury molecule 1 kidney injury molecule 1 8426 483 AF036335 N,E,F NonO/p54nrb homolog NonO/p54nrb homolog 17326 484 AF036548 N Rgc32 protein Rgc32 protein 17327 484 AF036548 N Rgc32 protein Rgc32 protein 15008 485 AF038591 E cytoplasmic aminopeptidase P cytoplasmic aminopeptidase P putative protein phosphatase 1 nuclear targeting 21491 486 AF040954 B subunit putative protein phosphatase 1 nuclear targeting subunit 22602 487 AF044574 M 2-4-dienoyl-Coenzyme A reductase 2, peroxisomal 2-4-dienoyl-Coenzyme A reductase 2, peroxisomal 22603 487 AF044574 N 2-4-dienoyl-Coenzyme A reductase 2, peroxisomal 2-4-dienoyl-Coenzyme A reductase 2, peroxisomal 20864 488 AF045464 N,B,J aflatoxin B1 aldehyde reductase aflatoxin B1 aldehyde reductase UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, 10241 489 AF048687 N,C,K polypeptide 6 UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase. polypetide 6 Table 1 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Title sodium channel, voltage-gated, type 8, alpha 117 490 AF049239 N polypeptide sodium channel, voltage-gated, type 8, alpha polypeptide 16649 491 AF051895 M,N,E annexin 5 annexin 5 985 492 AF053312 N small inducible cytokine subfamily A20 small inducible cytokine subfarmily A20 19058 493 AF054618 E cortactin isoform B cortactin isoform B 11843 494 AF054826 A vesicle-associated membrane protein 5 vesicle-associated membrane protein 5 17324 495 AF056031 M kynurenine 3-hydroxylase kynurenine 3-hydroxylase 4011 496 AF056333 N,J cylochrome P450, subfamily 2E, polypeptide 1 cytochrome P450, subfamily 2E, polypetide 1 1104 497 AF058714 N solute carrier family 13, member 2 solute carrier family 13, member 2 4589 498 AF062389 M,N,D kidney-specific protein (KS) kidney-specific protein (KS) 16006 499 AF062594 M nucleosome assembly protein 1-like 1 nucleosome assembly protein 1-like 1 16007 499 AF062594 N,E nucleosome assembly protein 1-like 1 nucleosome assembly protein 1-like 1 15761 500 AF062741 B pyruvate dehydrogenase phosphatase isoenzyme 2 pyruvate dehydrogenase phosphatase isoenzyme 2 nuclear RNA helicase, DECD variant of DEAD box 4327 501 AF063447 M,G,I family nuclear RNA helicase, DECD variant of DEAD box family 16444 502 AF065438 N peptidylprolyl isomerase C-associated protein peptidylprolyl isomerase C-associated protein 16155 503 AF068860 N defensin beta 1 defensin beta 1 25198 504 AF069782 M,N,I,K Nopp140 associated protein Nopp140 associated protein 17426 505 AF073839 C dynein-associated protein RKM23 dynein-associated protein RKM23 744 506 AF076856 M,N espin espin 5496 507 AF080468 M,N,D,E glucose-6-phosphatase, transport protein 1 glucose-6-phosphatase, transport protein 1 5497 507 AF080468 M,N,D,E glucose-6-phosphatase, transport protein 1 glucose-6-phosphatase, transport protein 1 25204 508 AF080507 N 10015 509 AF083269 M,G,K actin related protein 2/3 complex, subunit 1B actin related protein 2/3 complex, subunit 1B 10016 509 AF083269 M,G actin related protein 2/3 complex, subunit 1B actin related protein 2/3 complex, subunit 1B 20741 510 AF084186 A,J alpha-spectrin 2 alpha-spectrin 2 23679 511 AF087037 C,L B-cell translocation gene 3 B-cell translocation gene 3 15791 512 AF089817 C regulator of G-protein signaling 19 interacting protein 1 regulator of G-protein signaling 19 interacting protein 1 17535 513 AF090306 N,E retinoblastoma binding protein 7 retinoblastoma binding protein 7 16156 514 AF093536 N defensin beta 1 defensin beta 1 4723 515 AF093773 N malate dehydrogenase 1 malate dehydrogenase 1 2367 516 AF095741 N Mg87 protein Mg87 protein 2368 516 AF095741 N,K Mg87 protein Mg87 protein Table 1 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Title 6554 517 AF097723 N plasma glutamate carboxypeptidase plasma glutamate carboxypeptidase 15232 518 AI007622 D Rattus norvegicus transcribed sequences 24109 519 AI007725 J Rattus norvegicus transcribed sequences 15848 520 AI007820 N Rattus norvegicus heat shock protein 90 beta mRNA, partial sequence 1804 521 AI007824 L 6804 522 AI007877 M Rattus norvegicus transcribed sequences 15849 523 AI008074 N Rattus norvegicus heat shock protein 90 beta mRNA, partial sequence 16394 524 AI008106 K calcium binding protein A6 (Calcyclin) calcium binding protein A6 (calcyclin) Rattus norvegicus transcribed sequence with moderate similarity to protein pir:T44603 (H.sapiens) T44603 hypothetical protein CGI-83 [imported]- 3121 525 AI008160 M,G,K human solute carrier family 29 (nucleoside transporters), 11162 526 AI008183 C member 3 solute carrier family 29 (nucleoside transporters), member 3 Rattus norvegicus transcribed sequence with strong similarity to protein sp:P52209 (H.sapiens) 6PGD_HUMAN 6-phosphogluconate dehydrogenase, 23917 527 AI008441 H,I decarboxylating 22599 528 AI008458 M Rattus norvegicus transcribed sequences 22698 529 AI008578 L Rattus norvegicus transcribed sequences 19268 530 AI008641 D ribosomal protein L22 ribosomal protein L22 15434 531 AI008836 N high mobility group box 2 high mobility group box 2 low density lipoprotein receptor-related protein 410 532 AI008974 M,E associated protein 1 low density lipoprotein receptor-related protein associated protein 1 Rattus norvegicus transcribed sequence with strong similarity to protein sp:O95816 (H sapiens) BAG2_HUMAN BAG-family molecular chaperone 21632 533 AI009167 M,H,I regulator-2 Rattus norvegicus transcribed sequence with strong similarity to protein 6382 534 AI009362 M sp:P05423 (H sapiens) BN51_HUMAN BN51 protein 15097 535 AI009405 N insulin-like growth factor binding protein 3 insulin-like growth factor binding protein 3 10532 536 AI009602 K Rattus norvegicus transcribed sequences 23362 537 AI009605 N Ras homolog enriched in brain Ras homolog enriched in brain 895 538 AI009614 E Rattus norvegicus transcribed sequences 19358 539 AI009675 J Rattus norvegicus transcribed sequences 6833 540 AI009687 L Rattus norvegicus transcribed sequences Table 1 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Title 15089 541 AI009752 M,K Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with strong similarity to protein ref:NP_109630.1 (M.musculus) mesoderm development candidate 1 [Mus 6842 542 AI009764 K musculus] 15138 543 AI009801 C macrophage migration inhibitory factor macrophage migration inhibitory factor 17473 544 AI009806 M,N,K dynein, cytojplasmic, light chain 1 dynein, cytoplasmic, light chain 1 22619 545 AI009825 L Rattus norvegicus transcribed sequences 26133 546 AI009950 F 6869 547 AI010025 D Rattus norvegicus transcribed sequence 16824 548 AI010027 D Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with strong similarity to protein 21105 549 AI010067 M,F ref:NP_057032.1 (H.sapiens) CGI-19 protein [Homo sapiens] 12716 550 AI010178 M Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with weak similarity to protein 2912 551 AI010220 M,A,F sp: Q9Z1L1 (R.novegicus) CLD7_RAT CLAUDIN-7 13104 552 AI010224 D adducin 3, gamma adducin 3, gamma 17938 553 AI010332 C Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with weak similarity to protein 12095 554 AI010339 D ref:NP_077128.2 (M.musculus) ethanol induced 6 [Mus musculus] 6916 555 AI010430 M Rattus norvegicus transcribed sequences 18657 556 AI010435 K Rattus norvegicus transcribed sequences 16521 557 AI010470 B,J,L ceruloplasmin ceruloplasmin 6927 558 AI010542 M Rattus norvegicus transcribed sequences 17524 559 AI010568 M,A,I growth hormone receptor growth hormone receptor 21659 560 AI010584 D interferon induced transmembrane protein 3-like interferon induced transmembrane protein 3-like Rattus norvegicus transcribed sequence with weak similarity to protein 23509 561 AI010962 A ref:NP_445863.1 (R.norvegicus) sorting nexin 1 [Rattus norvegicus] 15679 562 AI011058 B,L Rattus norvegicus transcribed sequences 3934 563 AI011510 D Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with moderate similanty to protein 3941 564 AI011598 M,J sp:Q61001 (M.musculus) LMAS_MOUSE Laminin alpha-5 chain precursor 17550 565 AI011607 M,I trimethyllysine hydroxylase, epsilon trimethyllysine hydroxylase, epsilon 3995 566 AI011678 M,I,K syndecan 2 syndecan 2 Table 1 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Title 20804 567 AI011684 H transkelolase transketolase Rattus norvegicus transcribed sequence with strong similarity to protein 14267 568 AI011738 A sp:P38718 (R.norvegicus) P044_RAT 0-44 protein Rattus norvegicus transcribed sequence with strong similarity to protein ref:NP_114131.1 (H.sapiens) transmembrane protein induced by tumor 21060 569 AI011746 A necrosis factor alpha [Homo sapiens] 15616 570 AI011998 N dnaJ homolog. subfamily b, member 9 dnaJ homolog, subfamily b, member 9 13151 571 AI012030 M matrix Gla protein matrix Gla protein Rattus norvegicus transcribed sequence with moderate similarity to protein sp:Q9NXH9 (H.sapiens) TRMI_HUMAN Probable N(2),N(2)- dimethylguanosine tRNA methyltransferase (tRNA(guanine-26,N(2)-N(2)) methyltransferase) (tRNA 2,2-dimethylguanosine-26 methyltransferase) 6518 572 AI012114 M (tRNA(m(2,2)G26)dimethyltransferase) 17832 573 AI012182 J hemoglobin beta chain complex hemoglobin beta chain complex 21796 574 AI012221 M,I Seminal vesicle protein, secretion 2 Seminal vesicle protein, secretion 2 23946 575 AI012240 M Rattus norvegicus transcribed sequences 13633 576 AI012335 M activating transcription factor ATF-4 activating transcription factor ATF-4 2250 577 AI012354 M histone 2b histone 2b 24200 578 AI012356 M,B,L Rattus norvegicus transcribed sequences 7471 579 AI012379 L Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with strong similarity to protein ref:NP_006336.2 (H.sapiens) chromosome 4 open reading frame 1; 9116 580 AI012457 A,C expressed in human embryonic lung [Homo sapiens] 7127 581 AI012464 M Rattus norvegicus transcribed sequences (glutathione S-transferase, pi 2, glutathione-S- 20817 582 AI012589 M,N transferase, pi 1) (glutathione S-transferase, pi 2, glutathione-S-transferase, pi 1) 3493 583 AI012590 D,K Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with strong similarity to protein 3961 584 AI012598 A ref:NP_032333.1 (M.musculus) Hpall tiny fragments locus 9c [Mus musculus] 18713 585 AI012604 N,L eukaryotic initiation factor 5 (elF-5) eukaryolic initiation factor 5 (elF-5) 2242 586 AI012635 M,H,I,J flavin-containing monooxygenase 3 flavin-containing monooxygenase 3 7142 587 AI012689 C Rattus norvegicus transcribed sequences Table GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Known Gene name UniGene Cluster Title Rattus norvegicus transcribed sequence with strong similarity to protein sp:Q61188(M.musculus) EZH2_MOUSE Enhancer of zeste homolog 2 (ENX- 23810 588 AIO12781 E 1) 1409 589 AIO12802 M,A,C,E,F Hydroxyacyl glutathione hydrolase Hydroxyacyl glutathione hydrolase 20086 590 AIO13260 M,H lamin A lamin A Rattus norvegicus transcribed sequence with strong similarity to protein ref:NP_0350171 (M.musculus) NADH dehydrogenase (ubiquinone) Fe-S protein 4; NADH dehydrogenase (ubiquinone) Fe-S protein 4 (18 kDa) 9[Mus 21302 591 AIO13297 J musculus] 6758 592 AIO13394 B,L heparan sulfate (glucosamine) 3-O-sulfotransferase 1 heparan sulfate (glucosamine) 3-O-sulfotransferase 1 7270 593 AIO13564 D Rattus norvegicus Ab2-416 mRNA, complete cds 6674 594 AIO13568 I Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with strong similarity to protein 15159 595 AIO13697 D ref:NP_075918.1(M.musculus) RIKEN cDNA 6030432N09[Mus musculus] 7278 596 AIO13738 J Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with strong similarity to protein 22592 597 AIO13740 M,G,K ref:NP_062729.1( M.musculus) proteolipid protein 2 [Mus musculus] Rattus norvegicus transcribed sequence with strong similarity to protein 15928 598 AIO13829 M,K ref;NP_031947.1(M.musculus) E74-like factor 3 [Mus musculus] 21950 599 AIO13861 N,G 3-hydroxyisobulyrate dehydrogenase 3-hydroxyisobulyrate dehydrogenase 21391 600 AIO13902 M,K annexin A7 annexin A7 7299 601 AIO13911 M,A,B,L RNA binding motif protein 3 RNA binding motif protein 3 15904 602 AIO3971 F neurofascin neurofascin 815 603 AIO14087 N ribosomal protein S26 ribosomal protein S26 17908 604 AIO14163 M interferon-related developmental regulator 1 interferon-related developmental regulator 1 7216 604 AIO14165 A Rattusnorvegicus transcribed sequences 15247 606 AIO14169 N upregulated by 1,25-dihydroxyvitamin D-3 upregulated by 1,25-dihydroxyvitamin D-3 11326 607 AIO29015 F Rattus norvegicus transcribed sequences 22502 608 AIO29017 H putative zinc finger protein SERZ-1 putative zinc finger protein SERZ-1 12812 609 AIO29126 M,H Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with strong similarity to protein 3874 610 aIO29428 M,I pir:S50082 (H.sapiens) S50082 nuclear cap binding protein - human Table 1 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Title Rattus norvegicus transcribed sequence with moderate similarity to protein sp : P07814 (H. sapiens) SYEP_HUMAN Bifunctional aminoacyl-tRNA synthetase [Includes : Glutamyl-tRNA synthetase (Glutamate--tRNA ligase) ; 7451 611 A1029450 L Prolyl-tRNA synthetase (Proline--tRNA ligase)] 22415 612 A1029795 C growth response protein (CL-6) growth response protein (CL-6) 7537 613 A1029829 M Rattus norvegicus transcribed sequences 24893 614 A1029920 B insulin-like growth factor-binding protein 5 insulin-like growth factor-binding protein 5 7586 615 A1030024 C Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with weak similarity to protein ref : NP 446030. 1 (R. norvegicus) vacuolar proton-ATPase subunit M9. 2 2370 616 Al030179 M i [Rattus norvegicus] Rattus norvegicus transcribed sequence with strong similarity to protein ref : Nu-444391. 1 (M. musculus) mitochondrial ribosomal protein L27 [Mus 7634 617 A1030248 A musculus] 665 618 A1030430 B Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with strong similarity to protein ref : NP034922. 1 (M. musculus) methyltransferase-like 1 (S. cerevisiae) [Mus 7681 19 Al030449 J usculus] Rattus norvegicus transcribed sequence with strong similarity to protein 11559 620 A1030472 C ref : NP079615. 1 (M. musculus) RIKEN cDNA0610027018 [Mus musculus] Rattus norvegicus transcribed sequence with strong similarity to protein pir : JC5223 (M. musculus) JC5223 histidine--tRNA ligase (EC 6. 1. 1. 21)- 17419 621 A1030524 D mouse 7665 622 A1030668 E nucleosome assembly protein 1-like 1 nucleosome assembly protein 1-like 1 Rattus norvegicus transcribed sequence with weak similarity to protein sp : P43884 (R. norvegicus) PLIN RAT Perilipin (PERI) (Lipid droplet- 16169 623 A1030932 J associated protein) Rattus norvegicus transcribed sequence with strong similarity to protein 7825 624 A1031023 F pdb : 1 BGM (E. coli) 0 Chain 0, Beta-Galactosidase (Chains I-P) Rattus norvegicus transcribed sequence with strong similarity to protein 14856 625 A1043721 A pdb : 1 BGM (E. coli) 0 Chain 0, Beta-Galactosidase Chains I-P) 7896 626 A1043772 D Rattus norvegicus transcribed sequences 7903 627 A1043805 M Rattus norvegicus transcribed sequences Table 1 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Title 10818 628 A1043990 M, l Rattus norvegicus transcribed sequences 7964 629 A1044046 G Rattus norvegicus transcribed sequences 5430 630 A1044253 F Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with weak similarity to protein pir : S19586 (R. norvegicus) S19586 N-methyl-D-aspartate receptor glutamate- 5461 631 A1044338 M, B binding chain-rat 1431 632 A1044610 D dopa decarboxylase dopa decarboxylase Rattus norvegicus transcribed sequence with strong similarity to protein 2348 633 A1044794 M, D prf : 2208451B (M. musculus) 2208451B syntrophin [Mus musculus] 20983 634 A1044900 K fatty acid Coenzyme A ligase, long chain 2 fatty acid Coenzyme A ligase, long chain 2 21682 635 A1045030 N CCAAT/enhancerbinding, protein (C/EBP) delta CCAAT/enhancerbinding, protein (C/EBP) delta Rattus norvegicus transcribed sequence with moderate similarity to protein pir : A37086 (M. musculus) A37086 beta-galactosidase (EC 3. 2. 1. 23) precursor 19235 636 A1045074 M mouse Rattus norvegicus transcribed sequence with weak similarity to protein ref : NP 446417. 1 (R. norvegicus) solute carrier family 25 5711 637 A1045151 M (carnitine/acylcarnitine translocase), member 20 [Rattus norvegicus] 5474 638 A1045477 M Rattus norvegicus transcribed sequences 10004 639 A1045509 C Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with moderate similarity to protein 17755 640 A1045608 C, l pir : 160307 (E. coli) 160307 beta-galactosidase, alpha peptide-Escherichia coli 26173 641 Al045626 F 5855 642 A1045669 M Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with weak similarity to protein 23712 643 A1045827 L pir : T00043 (M. musculus) T00043 BH-protocadherin-a-mouse 5900 644 A1045866 I Rattus norvegicus transcribed sequences 7540 645 A1045882 M, B, L vitamin A-deficient testicular protein 5 vitamin A-deficient testicular protein 5 5329 646 A1045970 M amphiphysin amphiphysin Rattus norvegicus transcribed sequence with moderate similarity to protein 10069 647 A1058503 F sp : Q92537 (H. sapiens) Y247 HUMAN Hypothetical protein KIAA0247 8065 648 A1058509 B, L Rattus norvegicus transcribed sequence 8104 649 Al058655 B Table 1 GLGC GenBank Acc or Model Idenlifier Seq ID RefSeq ID Code Known Gene Name UniGeneCluster Title 8143 650 AIO58759 M Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with strong similarity to protein 4789 651 AIO58889 M pdb:1BGM (E. coli) o Chain O, Beta-Galaclosidase 9Chains I-P) 8188 652 AIO58943 M erythrocyte protein band 4.1-like 3 erythrocyte protein band 4.1-like 3 Rattus norvegicus transcribed sequence with moderate similarity to protein ref:NP_055702.1 (H.sapiens) hypothetical protein from BCRA2 region [Homo 8202 653 AIO58990 L sapiens] 8283 654 AIO59290 H Rattus norvegicus transcribed sequences 20802 655 AIO59508 N,H transketolase transketolase Rattus norvegicus transcribed sequence with moderale similarity to protein 3083 656 AIO60150 E ref:NP_003600.1(H.sapiens) HIRA-interacting protein 3[Homo sapiens] 9067 657 AIO70087 M prolactin prolactin Rattus norvegicus trascribed sequence with moderate similarity to protein ref:NP_444504.1 (H.sapiens) FKBP-associated protein isoform FAP68; 6343 658 AIO70108 A FK506-binding protein-associated protein [Homo sapiens] 8820 659 AIO70152 B,H,L Sms1 protein Smhs1 protein 26183 660 AIO70204 A Rattus norvegicus transcribed sequences 352 661 AIO70295 H growth arrest and DNA-damage-inducible 45 alpha growth arrest and DNA-damage-inducible 45 alpha Rattus norvegicus transcribed sequence with strong similarity to protein 24197 662 AIO70314 B,L pdb:1BGM(E. coli) O Chain O, Beta-Galactosidase (Chains I-P) 14424 663 AIO70421 M Rattus norvegious transcribed sequences 10434 664 AIO70497 B Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with strong similarity to protein 8927 665 AIO70523 A ref:NP_079737.1(M.musculus) RIKEN cDNA 18 10020G14[Mus musculus] 19031 666 AIO70532 M,L T-cell death associated gene T-cell death associated gene Rattus norvegicus transcribed sequence with strong similarity to protein 8944 667 AIO70597 F sp:Q9Y3A5 (H.sapiens) YC97_HUMAN Hypothetical protein CGI-97 8946 668 AIO70611 A Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with moderate similarity to protein ref:NP_067053.1(H.sapiens) myeloid/lymphoid or mixed-lineage leukemia 3; 10446 669 AIO70638 B ALR-like protein [Homo sapiens] Table 1 GLGC GenBank Acc or Model Identifier Seq ID ReefSEq ID Code Known Gene Name uniGene Cluster Title Rattus norvegicus transcribed sequence with strong similarity to protein 8739 670 AIO70859 D ref:NP_080044.1(M.musculus) GH regulated TBC protein 1 [Mus musculus] 9026 671 AIO70944 L Rattus norvegicus transcribed sequences 8721 672 AIO71024 M,A,D,I Rattus norvegicus transcribed sequence 9212 673 AIO71098 K tropomyosin isoform 6 tropomyosin isoform 6 18792 674 AIO71177 M,I Rattus norvegicus transcribed sequences 9583 675 AIO71185 M,C,L Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with strong similarity to protein 9079 676 AIO71251 B,I pir:A57050(M.musculus) A57050 K-glypican precursor - mouse 11057 677 AIO71509 L Rattus norvegicus transcribed sequences 22929 678 AIO71578 M,F neuronal regeneration related protein neuronal regeneration related protein 22930 678 AIO71578 M neuronal regeneration related protein neuronal regeneration related protein 9673 780 AOP81591 M,I Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with moderate similarity to protein ref:NP_071364.1 (H.sapiens) hypothetical protein bK1048E9.5 [Homo 8099 680 AIO71586 B sapiens] 11075 681 AIO71639 F Rattus norvegicus transcribed sequence 9699 682 AIO71646 M Rattus norvegicus transcribed sequences 9781 683 AIO71943 M,I Rattus norvegicus transcribed sequences 8665 684 AIO71965 C R.norvegicus hsp70.2 mRNA for heat shock protein 70 Rattus norvegicus transcribed sequence with moderate similarity to protein 12846 685 AIO72068 j pir:I60307 (E. coli) I60307 beta-galactosidase, alpha peptide - Escherihia coli 9191 686 AIO72107 A 10849 687 AIO72189 F Rattus norvegicus transcribed sequences 20003 688 AIO72362 M Rattus norvegicus transcribed sequences 21797 689 AIO72439 G,K Seminal vesicle protein, secretion 2 Seminal vesicle protein, secretion 2 1501 690 AIO72634 M,C,G,K keratin complex 1, acidic, gene 18 keratin complex 1, acidic, gene 18 9176 691 AIO72675 A dystonia 1, torsion (autosomal dominant; lorsin A) dystonia 1, lorsion (autosomal dominat; torsin A) 16813 692 AIO72746 I 19930 693 AIO72799 F Rattus norvegicus transcribed sequence 21885 694 AIO72886 M Rattus norvegicus transcribed sequences Table 1 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Known GeneName UniGene Cluster Title 9439 695 AIO72934 J Rattus norvegicus transcribed sequences 9468 696 AIO73021 M Rattus norvegicus transcribed sequences 24165 697 AI101113 F Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with weak similarity to protein sp:Q9JJ54 (R.norvegicus)ROD_RAT Heterogeneous nudear 6321 698 AI101256 M ribonucleoprotein D0 (hnRNP D0) (AU-rich element RNA-binding protein 1) 17734 699 AI101660 J Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with strong similarity to protein 4119 700 AI101901 L ref:NP_032404.1 (M.musculus) imprinted and ancient [Mus musculus] 2824 701 AI101999 C Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with strong similarity to protein sp:Q9QY73(M.musculus) C108_MOUSE Protein C1orf8 homolog precursor 18642 702 AI02023 C (Thymic dendrific cell-derived factor 1) 11953 703 AI102505 A cytochrome c oxidase, subunit VIIIa cytochrome c oxidase, subunit VIIIa Rattus norvegicus transcribed sequence with strong similarity to protein ref:NP_035792.1 (M.musculus) TYRO protein tyrosine kinase binding protein; 2125 704 AI102519 G killer cell activating receptor associated protein [Mus musculus] 15190 705 AI102562 M,N metallothionein metallothionein 19011 706 AI102618 L Rattus norvegicus transcribed sequences 23837 707 AI102620 M,N Rattus norvegicus transcribed sequences solute carrier family 20 (phosphate transporter), 23538 708 AI102727 M member 1 solute carrier family 20 (phosphate transporter), member 1 17234 709 AI102741 J Tissue inhibitor of metalloproteinase 3 Tissue inhibitor of metalloproteinase 3 Rattus norvegicus transcribed sequence with weak similarity to protein 17850 710 AI02750 H pir:JQ0866 (R.norvegicus) JQ0866 T-complex protein1 - rat 6796 711 AI102753 M,B ring finger protein 4 ring finger protein 4 4449 712 AI102838 N,B,G,K Isovaleryl Coenzyme A dehydrogenase Isovaleryl Coenzyme A dehydrogenase 8837 713 AI102849 C general transcription factor II I general transcription factor II I 15861 714 AI102868 N Rattus norvegicus phosphoserine aminotransferase mRNA, complete cds 16918 715 AI103074 N ribosomal protein S12 ribosomal protein S12 3584 716 AI103106 E lamin B1 lamin B1 3280 818 AI103224 F carbonyl reductase carbonyl reductase 13028 718 AI103253 A Rattus norvegicus transcribed sequences Table 1 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Title 1807 719 AI103365 L Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with moderate similarity to pretein pdb:1LBD(e. coli) B Chain B, Lactose Operon Repressor Bound To 21-Base 7622 720 AI103472 A Pair Symmetric Operator Dna, Alpha Carbons Only 20918 721 AI103552 J Rattus norvegicus transcribed sequences 4856 722 AI103708 G Rattus norvegicus transcribed sequences 16884 723 AI103758 E aldehyde dehydrogenase family 9, subfamily A1 aldehyde dehydrogenase family 9, subfamily A1 1649 724 AI103782 F Peptidylglycine alpha-amidating monooxygenase peptidylglycine alpha-amidating monooxygenase Rattus norvegicus transcribed sequence with strong similarity to protein ref:NP_079514.1 (H.sapiens) BTB (POZ) domain containing 1 [Homo 22885 725 AI103828 M,B sapiens] Rattus norvegicus transcribed sequence with strong similarity to protein pir:A32296 (R.norvegicus) A32296 ubiquinol-cytochrome-c reductase (eC 15050 726 AI103911 I 1.10.2.2) Rieske iron-sulfur protein precursor - rat (fragment) 7128 727 AI103937 M Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with moderate similarity to protein ref:NP_444393.1(M.musculus) mitochondrial ribosomal protein L36 [Mus 22271 728 AI103947 F musculus] 12450 729 AI103955 C LRP16 protein LRP16 protein 19991 730 AI103956 K mitochondrial aconitase (nuclear aco2 gene) mitochondrial aconitase (nuclear aco2 gene) Rattus norvegicus transcribed sequence with strong similarity to protein 20833 731 AI104035 N,A ref:NP_079904.1(M.musculus) RIKEn cDNA 2010000G05[Mus musculus] Rattus norvegicus transcribed sequence with moderate similarity to protein 22101 732 AI104251 M,C,I ref;NP_056222.1(H.sapiens) DKFZP564O243 protein [Homo sapiens] 4235 733 AI104524 M,H,K,L heterogeneous nuclear ribonucleoprotein A/B heterogeneous nuclear ribonucleoprotein A/B 18509 734 AI014528 A Rattus norvegicus DD6C4-4 mRNA, partial sequence Rattus norvegicus transcribed sequence with strong similarity to protein ref:NP_079411.1(H.sapiens) hypothetical protein KIAA1695; hytpthetical 12798 735 AI104773 M protein FLJ22297;KIAA1695 protein [Homo sapiens] Rattus norvegicus transcribed sequence with moderate similarity to protein 11232 736 AI104864 F ref:NP_076952.1(H.sapiens) hypothetical protein MGC3037 [Homo sapiens] Table 1 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Known Gene Name uniGene Cluster Title Rattus norvegicus transcribed sequence with moderate similarity to protein 16887 737 AI104883 F ref:NP_080841.1(M.musculus) RIKEN cDNA 9430083G14 [Mus musculus] Rattus norvegicus transcribed sequence with moderate similarity to protein sp:P48024 (M.musculus) SUI1_MOUSE Protein translation factor SUI1 21253 738 AI105110 F homolog 16885 739 AI105188 K aldehyde dehydrogenase family 9, subfamily A1 aldehyde dehydrogenase family 9, subfamily A1 10877 740 AI105198 N solute carrier family 34, member 1 solute carrier family 34, member 1 Rattus norvegicus transcribed sequence with moderate similarity to protein ref:NP_076133.1 (m.musculus) methylccrotonoyl-Coenzyme A carboxylase 1 5199 741 AI105272 M,G (alpha)[Mus musculus] 15364 742 AI105348 J cofilin 1 cofilin 1 7049 743 AI105371 C Rattus norvegicus transcribed sequences 7700 744 AI105383 M,D sphingosine kinase 1 sphingosine kinase 1 13343 745 AI105398 M Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with moderate similarity to protein pdg:1LBG (e. coli) B Chain B, Lactose Operon Repressor Bound To 21-Base 17221 746 AI105429 K Pair Symmetric Operator Dna, Alpha Carbons Only 23660 747 AI105448 N hydroxysteroid 11-beta dehydrogenase 1 hydroxysteroid 11-beta dehydrogenase 1 15291 748 AI111401 D multiple inositol polyphophate histidine phosphalase 1 multiiple inosilol polyphosphate histidine phosphalase 1 Rattus norvegicus Class II MHC RT1.D(a) beta chain precursor (RT1.D(a)) 16718 749 AI111537 H mRNA, complete cds 4479 750 AI111599 M growth arrest specific 5 growth arrest specific 5 Rattus norvegicus transcribed sequence with moderate similarity to protein 24211 751 AI111853 G sp:P06351 (M.musculus) H33_HUMAN Histone H3.3 (H3.A) (H3.B) (H3.3Q) Rattus norvegicus transcribed sequence with moderate similarity to protein 12925 752 AI111970 B pir:I60307 (E. coli) I6037 beta-galactosidase, alpha peptide - Escherichia coli 9017 753 AI112138 M Rattus norvegicus transcribed sequences 11198 754 AI112199 F Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with moderate similarity to protein ref:NP_071348.1 (H.saplens) hypothelical protein FLJ21877, death receptor- 12945 755 AI112212 F interacting protein [Homo sapiens] Table 1 GLGC GenBank Acc or model Identifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Title 20919 756 AI112516 N zinc finger protein 36, C3H type-like 1 zinc finger protein 36, C3H type-like 1 Rattus norvegicus transcribed sequence with moderate similarity to protein ref:NP_112595.1(H.sapiens) hypothelical protein DKFZp564B1162[Homo 3713 757 AI112571 M,J sapiens] proteasome (prosome, macropain) subunit, alpha type 15538 758 AI112633 L 6 proteasome (prosome, macropain) subunit, alpha type 6 Rattus norvegicus transcribed sequence with moderate similarity to protein pir:A57501 (M.musculus) A57501 uridine phosphorylase (eC 2.4.2.3)@- 12921 759 AI112636 M,B,L mouse Rattus norvegicus transcribed sequence with moderate similarity to protein pdb:1LBG(E. coli) B chain B, lactose Operon Represor Bound To 21-Base 13013 760 AI136233 B Pair symmetric Operator Dna, Alpha Carbons Only Rattus norvegicus transcribed sequence with weak similarity to protein ref:NP_064411.1 (M.musculus) Bat2; DNA segment, Chr 17, human D6S51E; 13020 761 AI136338 F RIKEN cDNA 3110039B05 gene [Mus musculus] Rattus norvegicus transcribed sequence with weak similarity to protein 9504 762 AI13723 F sp:O88553 (R.norvegicus) ZF37_RAT Zinc finger protein 37 (Zfp-37) 20920 763 AI136891 N zinc finger protein 36, C3H type-like 1 zinc finger protein 36, C3H type-like 1 13091 764 AI136977 L FK506 binding protein 4 (59 kDa) FK506 binding prootein 4 (59 kDa) 14638 765 AI137049 J nibrin nibrin Rattus norvegicus transcribed sequence with moderate similarity to protein 11937 766 AI137218 I ref:NP_076977.1 (H.sapiens) hypothetical protein MGC2835[Homo sapiens] 13111 767 AI137224 M oxysterol binding protein-like 1A oxysterol binding protein-like 1A 5290 768 AI137227 D Rattus norvegicus transcribed sequences 14142 769 AI137435 K Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with strong similarity to protein sp:P58006 (M.musculus) SES1_MOUSE Sestrin 1 (p53-regulated protein 6638 770 AI137579 M PA26) 16510 771 AI137583 N 7414 772 AI137586 K Table 1 GLGC GenBank Acc or Model identifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Title Rattus norvegicus transcribed sequence with weak similarity to protein sp:P48026 (M.musculus) ATDA_MOUSE Diamine acelyltransferase (Spermidine/spermine N(1)-acetyltransferase)(SSAT)(Putrescine 13157 773 AI138020 D acetyltransferase) 2264 774 AI144741 F Rattus norvegicus transcribed sequences 14458 775 AI145095 M Rattus norvegicus transcribed sequences 3610 776 AI145151 M,G,I,J histamine N-methyltransferase histamine N-methyltransferase 16227 777 AI145177 F early growth response 4 early grwth response 4 165 778 AI45329 F malate dehydrogenase, mitochondrial malate dehydrogenase, mitochondrial 8339 778 AI145761 M Rattus norvegicus Ac2-202 mRNA, complete cds 5531 780 AI45859 F Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with moderate similarity to protein 18522 781 AI145870 A,F,I ref:NP_075969.1(M.musculus) RIKEN cDNA 1110025H10 [Mus musculus] Rattus norvegicus transcribed sequence with strong similarity to protein sp:Q9WU56 (M.musculus) TRUA_MOUSE tRNA pseudouridine synthase A 2059 782 AI146005 A,H (Pseudouridylate synthase I) (Pseudouridine synthase I) (Uracil hydrolyase) 18503 783 AI169021 G calbindin 1 calbindin 1 Rattus norvegicus transcribed sequence with strong similarity to protein sp:Q9R0Q9 (M.musculus)MPU1_MOUSE Mannose-P-dolichol utilization defect 1 protein (Suppressor of Lec15 and Lec35 glycosylation mutation 23748 784 AI69037 F homolog) (SL15) Rattus norvegicus transcribed sequence with strong similarity to protein 5369 785 AI169058 A sp:Q13438 (H.sapiens) OS9_HUMAN protein OS-9 precursor solute carrier family 7 (cationic amino acid transporter, 7300 786 AI169077 C y+system), member 7 solute carrier family 7 (cationic amino acid transporter, y+system), member 7 11618 787 AI169115 M,C,F,@ Rattus norvegicus transcribed sequences 5920 788 AI169163 B Na/Pi cotransporter 4 Na/PI cotransporter 4 Rattus norvegicus transcribed sequence with strong similarity to protein sp:P46694 (M.musculus) IeX1_MOUSE Radiation-inducible immediate-early gene IEX-1 (Immediate early protein GLY96) (Immediate early response 3 12979 789 AI169177 M,B,H,I,L protein) 6290 790 AI169232 C kinase D-interacting substance of 220 kDa kinase D-interacting substance of 220 kDa Table 1 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code known Gene Name uniGene Cluster Title 15002 791 AI169327 M,E,G,K tissue inhibitor of metalloproteinae 1 tissue inhibitor of metalloproteinase 1 15003 791 Al169327 G,K tissue inhibitor of metalloproteinase 1 tissue inhibitor of metalloproteinase 1 17160 792 AI169370 N alpha-tubulin alpha-lubulin Rattus norvegicus transcribed sequence with weak similarity to protein 16338 793 AI69374 D ref:NP_075794.2(M.nusculus0 ubiquitin-associated protein [Mus musculus] Rattus norvegicus transcribed sequence with moderate similarity to protein 8234 794 AI169517 B ref:NP_060972.1 (H.sapiens) hypothetical protein PRO1580 [Homo sapiens] 24592 795 AI169622 D serine profease inhibitor, Kazal type 1 serine protease inhibitor, Kazal type 1 Rattus norvegicus transcribed sequence with weak similarity to protein 10839 796 AI169655 G ref:NP_035061.1 (M.musculus) nuclear protein 95 [Mus musculus] 12682 797 AI169656 D solute carrier family 22 member 8 solute carrier family 22 member 8 11429 798 AI169706 H ceroid-lipofuscinosis, neuronal 2 ceroid-lipofuscinosis, enuronal 2 8749 799 AI169802 N ferritin, heavy polypeptide 1 ferritin, heavy polypeptide 1 3916 800 AI169947 M,I Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with strong similarity to protein 16898 801 AI170249 B ref:NP_061367.1 (M.musculus) G21 protein [Mus musculus] 14929 802 AI170353 M,G,K ribosomal protein L21 ribosomal protein L21 Rattus norvegicus transcribed sequence with strong similarity to protein sp:O54931 (M.musculus) AKA2_MOUSE A-kinase anchor protein 2 (Protein Kinase A anchoring protein 2) (PRKA2) (AKAP expressed in kidney and lung) 5297 803 AI170379 M,D (AKAP-KL) 18687 804 AI170568 N dodecenoyl-coenzyme A delta isomerase dodecenoyl-coenzyme A delta isomerase 2534 805 AI170632 D,K Rattus norvegicus transcribed sequences 15393 806 AI170663 J gap junction membrane channel protein alpha 1 gap junction membrane channel protein alpha 1 10130 807 AI170759 M,A,I Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with moderate similarity to protein sp:Q04637 (H.sapiens) IF4G_HUMAN Eukaryotic translation initiation factor 4 3803 808 AI170773 A gamma (eIF-4-gamma) (eIF-4G) (elF4G) (P220) 2812 808 AI171090 J 3-hydroxy-3-methylglutaryl CoA lyase 3-ydroxy-3-methylglutaryl CoA lyase 22985 810 AI170193 A,F Rattus norvegicus transcribed sequences a disintegrin and metalloproteinase with a disintegrin and metalloproteinase with thrombospondin motifs 1 (ADAMTS- 22626 811 AI171159 M,K thrombospondin motifs 1 (ADAMTS-1) 1) Table 1 GLGC GenBank Acc r Identifier Seq ID RefSeq ID Code known Gene Name uniGene Cluster Title Rattus norvegicus transcribed sequence with weak similarity to protein pdb:1DT7(R.norvegicus) A Chain A, Solution Structure Of The C-Terminal Negative Regulatory Domain OF P53 in A Complex With Ca2+-Bound 736 812 AI171314 G S100b(Bb) Rattus norvegicus transcribed sequence with strong similarity to protein ref:NP_473384.1 (M.musculus) Musashi homolog 2 (Drosophila) [Mus 13285 813 AI171361 A musculus] 20828 814 AI171462 M,E,K CD24 antigen CD24 antigen Rattus norvegicus transcribed sequence with moderate similarity to protein pdb:1LBG(E. coli)B Chain B, Lactose Operon Repressor Bound To 21-Base 11761 815 AI71526 A Pair Symmetric Operator Dna, Alpha Carbons Only Rattus norvegicus transcribed sequence with strong similarity to protein 8215 816 AI71692 D pir:S48737 (R.norvegicus) S48737 kynurenine amintranferase - rat 10087 817 AI171803 M methylmalonate semialdehyde dehydrogenase gene methylmalonate semialdehyde dehydrogenase gene 11708 818 AI171807 M Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with moderate similarity to protein 22747 819 AI171832 M ref:NP_079752.1 (M.musculus) RIKEN cDNA 2410005O16 [Mus musculus] 7197 820 AI171962 M,G,K,L annexin 1 annexin 1 21956 821 AI171980 L Rattus norvegicus transcribed sequences 11205 822 AI172057 G Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with weak similarity to protein sp:P07825 (R.norvegicus) SYPH_RAT SYNAPTOPHYSIN (MAJOR 6630 823 ai172184 f SYNAPTIC VESICLE PROTEIN P38) Rattus norvegicus transcribed sequence with strong similarity to protein sp:Q9CWP8 (M.musculus) DPD4_MOUSE DNA polymerase delta subunit 4 3698 824 AI172193 C (DNA polymerase delat subunit p12) Rattus norvegicus transcribed sequence with weak similarity to protein sp:Q9WUK2 (M.musculus) IF4H_MOUSE Eukaryotic translation initiation factor 4H (eIF-4H)(Williams-Beuren syndrome chromosome region 1 protein 18681 825 AI172206 J homolog) Rattus norvegicus transcribed sequence with weak similarity to protein sp:P02773 (R.norvegicus) FETA_RAT Alpha-fetoprotein precursor (Alpha- 11968 826 AI172208 F fetoglobulin) (alpha-1-fetoprotein) Table 1 GLGC GenBank Acc or Model identifier Seq ID RefSeq ID Code Known Gene Name UniGene Gluster Tille 21975 827 Al172247 N,B,L xanthine dehydrogenase xanthine dehydrogenase 21842 828 Al172293 N sterol-C4-methyl oxidase-lkie slerol-C4-methyl oxidase-like Rattus norvegicus transcribed sequence with weak similanity to protein 15382 829 Al172302 M,H pir:S43056(M.musculus)S43058 hypothetical protein-mouse 17887 830 Al172414 J brain protein 44-like brain protein 44-like 13106 831 Al172615 D Rathus norvegicus transcribed sequences 13457 832 Al175319 F Rathus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with weak similanity to protein sp:P20171(R.norvegicus)RASH_RAT TRANSF ORMING PROTEIN P21/H- 4445 833 Al175466 G RAS-1 (C-H-RAS) 15683 834 Al175566 M t-comples testis expressed 1 t-comples testis expressed 1 22352 835 Al175959 M,H v-jun sarcoma virus 17 oncogene homolog (avian) v-jun sarcoma virus 17 oncegene homolog (avian) 22311 836 Al176007 B Rathus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with strong similanity to protein 17223 837 Al176140 D ret:NP_077751.1(M.musculus) testis expressed gene 189 [Mus musculus] 6782 838 Al176170 B FK506-binding prtein 1a FK506-binding protein 1a Rattus norvegicus transcribed sequence with strong similanity to protein pir:S41115(H.sapiens)S41115 probable flavoprotein-ubliquinone 17921 839 Al76422 F oxidoreductase (EC 1.6.5.-)- human Rattus norvegicus transcribed sequence with strong similanity to protein 15191 840 Al176456 M,N,F,L sp:P04355 (R.norvegicus)MT2_RAT METALLOTHIONEIN-II (MT-II) 21088 841 Al176472 A Rathus norvegicus transcribed sequences 24236 842 Al176473 M Rathus norvegicus transcribed sequences 18418 843 Al176483 D Rathus norvegicus transcribed sequences 20717 844 Al176504 N glutaminase glutaminase 16518 845 Al176546 N,C,K heat shock protein 86 heat shock prtein 86 3431 846 Al176595 N Calhepsin L Cathepsin L 17516 847 Al176621 A,E,L iron-responsive element-binding protein iron-responsive element-binding protein 17735 848 Al176658 C,K heal shock 27kDa protein 1 heal shock 27kDa protein 1 23299 849 Al176839 M Rathus norvegicus transcribed sequences Rathus norvegicus transcribed sequences with moderate similarily to protein 22103 850 Al176849 L sp:Q92503 (H.sapiens) SC14_HUMAN SEC14-like protein 1 15146 851 Al176969 M,K Rathus norvegicus transcribed sequences Table 1 GLGC GenBank Acc or Model idenlifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Title 20873 852 Al177042 G Rattus norvegicus DD6G4-2 mRNA, partial sequence Rathus norvegicus transcribed sequences with moderate similarily to protein 23018 853 Al177093 D ref:NP_038755.1(M.musculus) 5-azacytidine induced gene 2 (Mus musculus) Rathus norvegicus transcribed sequences with weak similarily to protein pir:S49158(R.norvegicus)S49158 complement protein C1q beta chain 13310 854 Al177119 L precursor - rat Rathus norvegicus transcribed sequences with weak similarily to protein 14083 855 Al177181 C ref:NP_076976.1(H.sapiens)hypothetical protein MGC2550 [Homo sapiens] M,A,B,H,I, 15964 856 Al177360 K,L Rathus norvegicus transcribed sequences 14989 857 Al177366 M,K Integrin, beta 1 Integrin, beta 1 14978 858 Al177386 F protein tyrosine phosphatase, receptor type, D protein tyrosine phosphatase, receptor type, D Rathus norvegicus transcribed sequences with strong similarily to protein 4987 859 Al177428 F ref:NP_055556.1(H.sapiens) AIAA0652 gene product [Homo sapiens] 18095 860 Al177482 D chaperonin subunit 4 (delta) chaperonin subunit 4 (delta) 15642 861 Al177503 M,F,J H3 histone, family 3B H3 histone, family 3B 150 862 Al177510 F Rathus norvegicus transcribed sequences 17470 863 Al177683 N,C,E Rattus norvegicus mRNA for hnRNP protein, partial 14425 864 Al177755 M,L pre-B-cell colony-enhancing facter pre-B-cell colony-enhancing facter Rathus norvegicus transcribed sequences with weak similarily to protein ref:NP_062100.1(R.norvegicus) intersectin (SH3 domain protein 1A) [Rattus 14484 865 Al177867 M norvegicus] Rathus norvegicus transcribed sequences with strong similarily to protein 3834 866 Al177902 G ref:NP_080665.1 (M.musculus) RIKEN cDNA 1300003F06[MUs mustculus] Rathus norvegicus transcribed sequences with moderate similarily to protein pir:S23251(M.musculus)S23251 protein-tyrosine kinase(EC 2.7.1.112) ark 5929 867 Al177962 E precursor-mouse 17833 868 Al177992 F hemogiobin beta chain complex hemogiobin beta chain complex Rathus norvegicus transcribed sequences with strong similarily to protein sp:P70284(M.musculus)TGIF_MOUSE 5'-TG-3' INTERACTING FACTOR 19184 869 Al178025 M,H,I (MOHMEOBOX PROTEIN TGIF) Table 1 GLGC GenBank Acc or Model identifier Seq ID RefSeq ID Code Known Gene Name UniGene Gluster Tille Complement component 1, q subcomponent binding 15259 870 Al178135 N protein Complement component 1, q subcomponent binding protein Rathus norvegicus transcribed sequences with moderate similarily to protein pir:T13963(M.musculus)T13963 formin related protein, lymphocyle specific- 6059 871 Al178245 M,J mouse Rathus norvegicus transcribed sequences with strong similarily to protein 18996 872 Al178326 J ref:NP_077291.1(H.sapiens)hypothetical protein MGC4175[Homo sapiens] 8445 873 Al178394 J Rathus norvegicus transcribed sequences Rattus norvegicus clone D920 inteslinal epithelium proliferating cell- 22197 874 Al178527 M,H associated mRNA sequence 17563 875 Al178750 N eukaryolic translation elongation factor 2 eukaryolic translation elongation factor 2 Rathus norvegicus transcribed sequences with weak similarily to protein sp:Q10758(R.norvegicus)K2C8_RAT keralin, type II cytoskeletal 8 22648 876 Al178996 A (Cytokeratin 8)(Cylokeratin endo A) 14983 877 Al179150 D Rathus norvegicus transcribed sequences with strong similarily to protein 8477 878 Al179167 M pdb:18GM(E. coli) O Chain O, Beta-Galaclosidase (Chains I-P) 13611 879 Al179378 M,F,H protease, serine, 8 (prostaasin) protease, serine, 8 (prostasin) 13634 880 Al179381 M activating transcription factor ATF-4 activating transcription factor ATF-4 Rathus norvegicus transcribed sequences with weak similarily to protein sp:O75643 (H.sapiens)U520_HUMAN U5 small nuclear ribonucleoprotein 13607 881 Al179403 H 200 kDa helicase (U5 snRNP-specific 200 kDa protein)(U5-200KD) 13614 882 Al179407 B,L Rathus norvegicus transcribed sequences 15042 883 Al179422 M Rathus norvegicus transcribed sequences 17829 884 Al179576 N,J heoglobin beta chain complex heoglobin beta chain complex 23151 885 Al179595 B,L FXYD domain-containing ion transport regulator 6 FXYD domain-containing ion transport regulator 6 19822 886 Al179599 A Ras-related GTP-binding protein Rab29 Ras-related GTP-binding protein Rab29 5901 887 Al179605 D Rathus norvegicus transcribed sequences 16081 888 Al179610 N Hemoxygenase Heme oxygenase 3049 889 Al179892 M lipocalin 7 lipocalin 7 1687 890 Al179971 J hemoglobin, alpha 1 hemoglobin, alpha 1 Table 1 GLGC GenBank Acc or Model identifier Seq ID RefSeq ID Code Known Gene Name UniGene Gluster Tille Rathus norvegicus transcribed sequences with weak similarily to protein ref:NP_077349.1(R.norvegicus) polypeptide GalNc transferase T1[Rattus 22569 891 Al179979 M.I norvegicus] Rathus norvegicus transcribed sequences with strong similarily to protein pir:S50853(H.sapiens) S50853 translation releasing factor eRF-1 [validated]- 5481 892 Al180170 M human Rathus norvegicus transcribed sequences with weak similarily to protein sp:Q9JLT0(r.norvegicus)MYHA_RAT Myosin heavy chain, nonmusde type B (Cellular myosin heavy chain, type B)(Nonmuscle myosin heavy chain-B) 6765 893 Al227761 M,H,I (NMMHC-B) 6487 894 Al227919 M Rathus norvegicus transcribed sequences 19188 895 Al227938 G,J Rathus norvegicus transcribed sequences 1651 896 Al228068 A,H Peptidlglycine alpha-amidating monooxygenase Peptidylglycine alpha-amidating monooxygenase Rathus norvegicus transcribed sequences with strong similarily to protein 16913 897 Al228236 E ref:NP_062308.1(M.musculus)neuronal protein 15.6(Mus musculus) 15879 898 Al228313 M,K Rathus norvegicus transcribed sequences Rathus norvegicus transcribed sequences with weak similarily to protein 13727 899 Al228326 M,A ref:NP_491986.1(C.elegans)C30F12.2.p(Caenorhabditis elegans) 6102 900 Al228335 L Rathus norvegicus transcribed sequences Rathus norvegicus transcribed sequences with weak similarily to protein prf:2112356A(R.norvegicus)2112356A hepalocyte nuclear factor (Rattus 17892 901 Al228438 H norvegicus] Rathus norvegicus transcribed sequences with moderate similarily to protein 13740 902 Al228455 A ref:NP_037457.2(H.sapiens)KIAA0943 prolein [Homo sapiens] Rathus norvegicus transcribed sequences with strong similarily to protein 1474 903 Al228548 N sp:P35467(R.novegicus0S10A_RAT S-100 protein, alpha chain 18612 904 Al228624 G ribosomal protein L29 ribosomal prolein L29 13176 905 Al228654 M Rathus norvegicus transcribed sequences 4392 905 Al228674 H Peptidylproly isomerase A(cyclophilin A) Peptidylproly isomerase A(cyclophilin A) 15296 907 Al228738 N,H,I (FK506 binding prolein 2, FK506-binding protein 1a) (FK506 binding prolein 2, FK506-binding protein 1a) 22328 908 Al229142 M Rathus norvegicus transcribed sequences Table 1 GLGC GenBank Acc or Model idenlifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Title Rattus norvegicus transcribed sequence with weak similanity to protein sp: P06399 (R.norvegicus) FIBA_RAT Fibringon alpha/plpha-E chain 7892 909 AI229172 K precursor 6886 910 AI229332 F Rattus norvegicus transcribed sequence Rattus norvegicus transcribed sequence with weak similanity to protein ref:NP_061898.1 (H.sapiens) chromosome 20 open reading frame 16 (Homo 23435 911 Al229502 H,I sapiens) 17448 912 Al229637 N MYB binding protein 1a MYB binding protein 1a Rattus norvegicus transcribed sequence with weak similanity to protein ref:NP_004542.1 (H.sapiens) NADH dehydrogenase (ubiquinone) Fe-S 3099 913 Al229680 E protein 3 (30kD)(NADH-coenzyme Q reductase)(Homo sapiens) 1652 914 Al229728 A Peplidylglycine alpha-amidating monooxygenase Peplidylglycine alpha-amidating monooxygenase 9035 915 Al229879 F,J Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with weak similanity to protein 11866 916 Al229966 F ref:NP_032776.1(M.musculus) nucleoredoxin (Mus musculus) Rattus norvegicus transcribed sequence with weak similanity to protein sp:Q63344(R.norvegicus)MOT2_RAT Monocarboxylate transporter 2 (MCT 12587 917 Al229979 M 2) 24042 918 Al230002 C Rattus norvegicus transcribed sequence 12551 919 Al230056 C,K Rattus norvegicus transcribed sequence Rattus norvegicus transcribed sequence with weak similanity to protein 6629 920 Al230165 D ref:NP_057038.1(H.sapiens) CGI-26 prolein (Homo sapiens) 15862 921 Al230228 N Rattus norvegicus phosphoserine aminotransterase mRNA, complete cds 4280 922 Al230247 F selenoprolein P, plasma, 1 selenoprolein p, plasma, 1 Rattus norvegicus transcribed sequence with weak similanity to protein 14450 923 Al230252 B sp:Q13045(H.sapiens)FLIH_HUMAN Flighties-I protein homolog 18528 924 Al230284 K Tropomycin 4 Tropomycin 4 20895 925 Al230549 H Rattus norvegicus transcribed sequence 12961 926 Al230554 M Rattus norvegicus transcribed sequence 24264 927 Al230712 M Subtilisin - like endoprotease Sublilisin - like endoprolease 18529 928 Al230716 M,K Tropomycin 4 Tropomycin 4 SAC1(supressor of aclin mulations 1, homolog)-like (S. 13618 929 Al230724 M,I cerevisiae) SAC1 (supressor of actin mutation 1, homolog)-like (S. cerevisiae) Table 1 GLGC GenBank Acc or Model identifier Seq ID RefSeq ID Code Known Gene Name UniGene Gluster Tille Rathus norvegicus transcribed sequences with strong similarily to protein pir:S42114(M.musculus)S42114 small nuclear ribonucieoprotein U1A- 24108 930 Al230728 G mouse Rathus norvegicus transcribed sequences with weak similarily to protein 21648 931 Al230880 J pir:JE0343(R.norvegicus)JE0343 terf protein - rat 1688 932 Al230970 J hemoglobin, aipha 1 hemoglobin, alpha 1 16087 933 Al231011 F Rathus norvegicus transcribed sequences 3125 934 Al231028 K erythrocyte protein band 4.1-like 1 erythrocyte protein band 4.1-like 1 13934 935 Al231044 F Rathus norvegicus transcribed sequences 15132 936 Al231180 G calcium-regulaled heat-stable protein (24KD) calcium-regulaled heat-stable protein (24KD) 18678 937 Al231295 L Rathus norvegicus transcribed sequences Rathus norvegicus transcribed sequences with strong similarily to protein 17268 938 Al231317 F ref:NP_080171.1 (M.mustculus) endothelial-derived gene [Mus musculus] 3050 939 Al231321 M lipocalin 7 lipocalin 7 13966 940 Al231421 B nuclear ubiquitous casein kinase 2 nuclear ubliquitous casein kinase 2 12343 941 Al231433 C Rathus norvegicus transcribed sequences 17196 942 Al231519 M,N,I sialyltransferase 7c sialyltransferase 7c Rathus norvegicus transcribed sequences with strong similarily to protein 13092 943 Al231547 L pir:S14538(M.musculus)S14538 transilion prolein - mouse Rathus norvegicus transcribed sequences with strong similarily to protein sp:Q9JLV1(M.musculus)BAG3_MOUSE BAG-family molecular chaparone 15171 944 Al231792 H regulator-3 (BCL-2 binding alhangogene-3)(BAG-3)(Bcl-2-binding protein Bis) 8211 945 Al231807 H ferritin light chain 1 ferritin light chain 1 8212 945 Al231807 N,L ferritin light chain 1 ferritin light chain 1 20702 946 Al231821 N stathmin 1 statmin 1 10789 947 Al232059 M aspartoacylase aspartoacylase Rathus norvegicus transcribed sequences with moderate similarily to protein 14020 948 Al232076 M ref:NP_076138.1(M.musculus)harmonin isoform a1 (Mus musculus) 573 949 Al232087 N,J hydroxyacid oxidase(glycolate oxidase) 3 hydroxyacid oxidase(glycolate oxidase) 3 12366 950 Al232088 F Rathus norvegicus transcribed sequences 15039 951 Al232096 M,F,1 solute carrier family 15, member 2 soulte carrier family 15, member 2 9332 952 Al232210 F MIC2 like 1 MIC2 like 1 Table 1 GLGC GenBank Acc or Model identifier Seq ID RefSeq ID Code Known Gene Name UniGene Gluster Tille low densily lipoprotein receptor-related protein 409 953 Al232268 M,N,I associated protein 1 low density lipoprotein receptor-related protein associated protein 1 15955 954 Al232294 M,G,I Rathus norvegicus transcribed sequences Rathus norvegicus transcribed sequences with moderate similarily to protein pdb:1LBG(E. coli) B Chain B, Lactose Operon Repressor Bound To 21-Base 15246 955 Al232332 D Pair Symmetric Operator Dna, Alpha Carbons Only 24321 956 Al232340 M,K,L chemokine(C-X-C motif) ligand 12 chemokine (C-X-C motif) ligand 12 Rathus norvegicus transcribed sequences with weak similarily to protein 16172 957 Al232341 K ref:NP_498462.1(C.elegans) C1389.2.p[Caenorhabdilis elegans) 5601 958 Al232461 M,I flavin containing monooxygenase 4 flavin containing monooxygenase 4 Rathus norvegicus transcribed sequences with strong similarily to protein 11157 959 Al232494 K pdb:1BGM(E. coli) O Chain O, Bela-Galactosidase (Chains I-P) 4440 960 Al232643 M,I Rathus norvegicus transcribed sequences Rathus norvegicus transcribed sequences with moderate similarily to protein 7285 961 Al232731 M ref:NP_080434.1(M.musculus)RIKEN CDNA 0610042E07 [Mus musculus] Rathus norvegicus transcribed sequences with weak similarily to protein sp:P97852(R.norvegicus)DHB4_RAT Estradiol 17 beta-dehydrogenase 4 (17- 17695 962 Al232784 E beta-HSD 4)(17-beta-hydroxysteroid dehydrogenae 4) (HSD IV) 12467 963 Al232924 M Rathus norvegicus transcribed sequences 19998 964 Al232999 M PDZ domain containing 1 PDZ domain containing 1 Rathus norvegicus transcribed sequences with weak similarily to protein sp:Q63413(R.norvegicus)HE47_RAT Probable ATP-dependent RNA 3823 965 Al233147 M helicase p47 11967 966 Al233155 M,J Rathus norvegicus transcribed sequences 13954 967 Al233209 M crystallin, mu crystallin, mu 4574 968 Al233216 N glulamate dehydrogenase 1 gluatamte dehdrogenase 1 17907 969 Al233224 M epidemal growth factor receptor epidemal growth factor receptor Rathus norvegicus transcribed sequences with moderate similarily to protein sp:P06684 (M.musculus)C05_MOUSE Complement C5 precursor (Hemolytic 10378 970 Al233300 A complement)[Contains: C5A anaphylatoxin] 14120 971 Al233433 K Rathus norvegicus transcribed sequences 19509 972 Al233437 L Rathus norvegicus transcribed sequences Table 1 GLGC GenBank Acc or Model identifier Seq ID RefSeq ID Code Known Gene Name UniGene Gluster Tille Rathus norvegicus transcribed sequences with weak similarily to protein ref:NP_542421.1(R.norvegicus) cask-interacting protein 1 [Rattus 14095 973 Al233468 M,I norvegicu] 14131 974 Al233490 L Rathus norvegicus transcribed sequences 6046 975 Al233530 M,B,I,L Rathus norvegicus transcribed sequences 7888 976 Al233583 M tissue inhibitor of metalloproteinase 2 tissue inhibitor of metalloproteinase 2 Rathus norvegicus transcribed sequences with strong similarily to protein ref:NP_542121.1(M.musculus) proteasome (prosome, macropain)26S 3816 977 Al233729 H subunit, non-ATPase, 5 [Mus musculus] 7804 978 Al233771 K Rathus norvegicus transcribed sequences 13563 979 Al233773 E MAWD binding protein MAWD binding protein 1653 980 Al233806 A Peplidylglycine alpha-amidating monooxygenase Peplidylglycine alpha-amidating monooxygenase 535 981 Al233916 E Rathus norvegicus transcribed sequences 13392 982 Al234146 M cysteine rich prolein 1 cysteine rich protein 1 Rathus norvegicus transcribed sequences with weak similarily to protein ref:NP_008958.1(H.sapiens) topoisomerase (DNA) Il binding protein [Homo 8325 983 Al234293 E sapiens] 6416 984 Al234295 M,K solute carrier family 34 (sodium phosphate), member 2 solute carrier family 34 (sodium phosphate), member 2 17764 985 Al234604 N heat shock protein 8 heat shock protein 8 Rathus norvegicus transcribed sequences with weak similarily to protein 14677 986 Al234620 M,G,K,L ref:NP-071796.1(R.norvegicus)plectin[Rattus norvegicus] Rathus norvegicus transcribed sequences with weak similarily to protein pir:JC7152(M.musculus)JC7152 UV-damaged DNA-binding 127K protein 22213 987 Al234858 K mouse Rathus norvegicus transcribed sequences with strong similarily to protein ref:NP_076401.1(M.musculus) ubiquilous protein kinase-like (105 kDa)[Mus 26319 988 Al234867 H musculus[ ubiquitin-conjugating enzyme E2D 2 (homologous to 15277 989 Al234889 D yeast UBC4/5) ubiquitin-conjugating enzyme E2D 2 (homologous to yeast UBC4/5) Rathus norvegicus transcribed sequences with strong similarily to protein 22662 990 Al234939 M ref:NP_076320.1(Mmusculus) RIKEN cDNA 1500035H01 [Mus musculus] 24649 991 Al234950 C,K acid phosphatase 2 acid phosphatase 2 Table 1 GLGC GenBank Acc or Model identifier Seq ID RefSeq ID Code Known Gene Name UniGene Gluster Tille Rathus norvegicus transcribed sequences with strong similarily to protein 3875 992 Al235047 M,A pir:S50082(H.sapiens)S50082 nuclear cap binding protein - human 8850 993 Al235059 B Rathus norvegicus transcribed sequences 15004 994 Al235224 M,G,K tissue inhibitor of metalloproteinase 1 tissue inhibitor of metalloprateinase1 Rathus norvegicus transcribed sequences with strong similarily to protein sp:P54577 (H.sapiens) SYY_HUMAN tyrostl-tRNA synthetase (Tyrosyl- 6632 995 Al235277 C tRNA ligase)(TyrRS) 896 996 Al235313 E Rathus norvegicus transcribed sequences 15468 997 Al235384 N ribosomal protein S15a ribosomal protein S15a 7937 998 Al235414 B Rathus norvegicus transcribed sequences 1462 999 Al235585 M,E,G cathepsin D cathepsin D Rathus norvegicus transcribed sequences with strong similarily to protein ref:NP_114131.1(H.sapiens) transmembrane protein induced by tumor 21061 1000 Al235631 M,A necrosis factor alpha (Homo sapiens) Rathus norvegicus transcribed sequences with moderate similarily to protein 11164 1001 Al235739 M,I pir:A56716(H.sapiens)A56716 aromatic ester hydrolase (EC 3.1.1.-)-human Rathus norvegicus transcribed sequences with weak similarily to protein ref:NP_071953.1(R.norvegicus)C1-tetrahydrofolate synthase [Rattus 7307 1002 Al235935 C,K norvegicus] Rathus norvegicus transcribed sequences with moderate similarily to protein ref:NP_004540.1(H.sapiens) NADH dehydrogenae 9ubiquinone) 1 15836 1003 Al235951 A subcomplex unknow. 2 (14, 5kD. B14,5b)[Homc sapiens[ 3091 1004 Al236027 M,A,C,H,I Rathus norvegicus transcribed sequences 14867 1005 Al236061 M Rathus norvegicus transcribed sequences Rathus norvegicus transcribed sequences with strong similarily to protein ref:NP_062416.1 (M.musculus) Down syndrome critical region protein c {mus 22855 1006 Al236150 A musculus] 13004 1007 Al236284 J,L fatty acid Coenzyme A ligase, long chain 4 fatty acid Coenzyme A ligase, long chain 4 15051 1008 Al236332 M Rattus norvegicus Ab2-402 mRNA, complete cds 1689 1009 Al236360 J hemoglobin, alpha 1 hemoglobin, alpha 1 Table 1 GLGC GenBank Acc or Model identifier Seq ID RefSeq ID Code Known Gene Name UniGene Gluster Tille siah binding protein 1; FBP interacting repressor; pyrimidine tract binding splicing factor, Ro siah binding protein 1; FBP interacting repressor; pyrimidine tract binding splicing 10667 1010 Al236366 C ribonuleoprotein-binding protein splicing factor, Ro ribonuclepoprolein-binding protein 1 783 1011 Al236589 F lipase, hormone sensitive lipase, hormone sensilive Rathus norvegicus transcribed sequences with strong similarily to protein sp:P22366 (M.musculus) MY88_MOUSE MYELOID DIFFERENTIATION 17950 1012 Al236590 L PRIMARY RESPONSE PROTEIN MYD88 Rathus norvegicus transcribed sequences with strong similarily to protein sp:Q61699(M.musculus)H105_MOUSE Heat-shock proteein 105 kDa(Heat shock-related 100 kDa protein E71)(HSP-E71)(Heat shock 110kDa protein) 18259 1013 Al236601 H (42 degrees C-HSP) 2574 1014 Al236616 F Rathus norvegicus transcribed sequences 16859 1015 Al236763 M,D Rathus norvegicus transcribed sequences 5208 1016 Al236754 G pregnancy-induced growth inhibitor pregnancy-induced growth inhibitor Rathus norvegicus transcribed sequences with weak similarily to protein ref:NP_113865.1(R.noregicus) four and a half LIM domains 2 [Rattus 24388 1017 Al236772 M,K norvegicus] 15850 1018 Al236795 N,K Rattus norvegicus heat shock protein 90 beta mRNA, parteial sequence 18303 1019 Al236863 M Rathus norvegicus transcribed sequences 19890 1020 Al237108 F Rathus norvegicus transcribed sequences Rathus norvegicus transcribed sequences with weak similarily to protein sp:P20695 (R.norvegicus)IFR1_RAT INTERFERON-RELATED DEVELOPMENTAL REGULATOR 1(NERVE GROWTH FACTOR- 23076 1021 Al237388 K INDUCIBLE PROTEIN PC4)(IRPR) 21653 1022 Al237535 M,C,K LPS-induced TNF-alpha factor LPS-induced TNF-alpha factor 3615 1023 Al237645 J Rathus norvegicus transcribed sequences 8759 1024 Al237646 B,L Rathus norvegicus transcribed sequences Rathus norvegicus transcribed sequences with moderate similarily to protein sp:O09015(R.norvegicus)MXI1_RAT MAX interacting protein 1 (MXH 3467 1025 Al237835 M,I protein) 6127 1026 Al638960 A Rathus norvegicus transcribed sequences 11692 1027 Al638982 M,N sulfotransferase family, cytosolic, 1C, member 2 sulfotransferase family, cytosolic, 1C, member 2 Table 1 GLGC Genbank Acc or Model Identifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Title Rattus norvegicus transcribed sequence with moderale similarity to protein 20000 1028 AI638989 A,B pir:T14273 (M.musculus) T14273 zinc finger protein 106 - mouse Rattus norvegicus transcribed sequence with weak similarity to protein 23781 1029 AI639012 F ref:NP_076947.1 (H.sapiens) hypolhetical protein MGC2601 [Homo sapiens] 25862 1030 AI639022 A 19997 1031 AI639043 N Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with strong similarily to proten ref:NP_075371.1 (M.musoulus) Nedd4 WW binding# protein 4; Nedd4 WW- 10071 1032 AI639058 N,F binding protein 4 [Mus musculus] mini chromosome maintenance delicient 6 (S. 16676 1033 AI639082 N,E cerevisiae) mini chromosome maintenance deficient 6 (S. cerevisiae) 19952 1034 AI639108 N Rattus norvegious transcribed sequences 25902 1035 AI639154 H Rattus norvegious transcribed sequence 19112 1036 AI639157 J ribosomal protein L13 ribosomal protein L13 15379 1037 AI639162 N,B Rattus norvegious transcribed sequences 25907 1038 AI639167 N Rattus norvegious transcribed sequences 25921 1039 AI639209 A,F 15330 1040 AI639285 M,F,I Rattus norvegious transcribed sequences Rattus norvegious transcribed sequence with strong similarity to protein sp:P58064 (M.musculus) RT06_MOUSE Mitochondrial 28S ribosomal protein 19152 1041 AI639387 M,D S6 (MRP-S6) 19679 1042 AI639418 M,A,D,G,I deiodinase, iodothyronine, type I deiodinase, iodothyronine, type I 19002 1043 AI639465 N ring finger protein 28 ring finger protein 28 19003 1043 AI639465 F ring finger protein 28 ring finger protein 28 Rattus norvegicus transcribed sequence with strong similarity to protein ref:NP_058622.1 (M.musculus) squamous cell carcinoma anligen recognized 21542 1044 AI639476 J by T-cells 3 [Mus musculus] Rattus norvegicus transcribed sequence with strong similarity to protein 19943 1045 AI639479 M,N,F,G prf:2008147A (R.norvegicus) 2008147A protein RAKb [Rattus norvegious] Rattus norvegicus transcribed sequence with strong similarity to protein 20082 1046 AI639488 M,N,H,I,J pir:A42772 (R.norvegicus) A42772 mdm2 protein - rat (fragments) 20056 1047 AI639504 M,I Rattus norvegicus Ac2-202 mRNA, complete cds Table 1 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Title Rattus norvegicus transcribed sequence with weak similarity to protein 15237 1048 AI639535 J ref:NP_445944.1 (R.norvegicus) transporter-like protein [Rattus norvegicus] 1203 1049 AJ000485 N cytoplasmic linker 2 cytoplasmic linker 2 25233 1050 AJ000556 E Janus kinase 1 Janus kinase 1 14332 1051 AJ001044 D tumor-associated calcium signal transducer 1 tumor-associated calcium signal transducer 1 25235 1052 AJ001290 F solute carrier family 5 (inositol transporters), member 3 solute carrier family 5 (inositol transporters), member 3 12422 1053 AJ006971 N Death-associated like kinase Death-associated like kinase 12423 1053 AJ006971 N Death-associated like kinase Death-associated like kinase 25247 1054 AJ011608 N DNA primase, p49 subunit DNA primase, p49 subunit 20404 1055 AJ011656 N,L claudin 3 claudin 3 16350 1056 AJ011811 G claudin 3 claudin 7 16351 1056 AJ011811 G claudin 3 claudin 7 13485 1057 AJ012603 B a disintegrin and metalloproteinase domain 17 a disintegrin and metalloproteinase domain 17 4290 1058 AJ224120 L peroxisomal membrane protein Pmp26p (Peroxin-11) peroxisomal membrane protein Pmp26p (Peroxin-11) 18956 1059 D00512 N acetyl-coenzyme A acetyltransferase 1 acetyl-coenzyme A acetyltransferase 1 15408 1060 D00569 N 2,4-dienoyl CoA reduclase 1, mitochondrial 2,4-dienoyl CoA reductase 1, mitochondrial 15049 1060 D00569 N,L 2,4-dienoyl CoA reduclase 1, mitochondrial 2,4-dienoyl CoA reductase 1, mitochondrial 4615 1061 D00680 N glutathione peroxidase 3 glutathione peroxidase 3 (Rattus norvegious mRNA for delta3, delta2-enoyl-CoA isomerase, complete 18686 1062 D00729 N dodecenoyl-coenzyme A delta isomerase cds, dodecenoyl-coenzyme A delta isomerase) 2554 1063 D00913 M,N intercellular adhesion molecule 1 intercellular adhesion molecule 1 2555 1063 D00913 M,C,I intercellular adhesion molecule 1 intercellular adhesion molecule 1 1515 1064 D10233 J renin-binding protein renin-binding protein 1306 1065 D10262 N choline kinase choline kinase 24821 1066 D10392 J syntaxin 1a syntaxin 1a 3608 1067 D10693 M,J histamine N-methyltransferae histamine N-methyltransferase 25253 1068 D10754 H proteasome (prosome, macropain) subunit, beta type 6 proteasome (prosome, macropain) subunit, beta type 6 proteasome (prosome, macropain) subunit, beta type 15535 1069 D10755 L 6 proteasome (prosome, macropain) subunit, beta type 6 proteasome (prosome, macropain) subunit, beta type 3254 1070 D10756 N,L 5 proteasome (prosome, macropain) subunit, beta type 5 Table 1 GLGC GenBank Acc or Model Identifier Seq ID RetSeq ID Code Known Gene Name UniGene Cluster Title proteosome (prosome, macropain) subunit, beta type 9 proteosome (prosome, macropain) subunit, beta type 9 (large multifunctional 4003 1071 D10757 N (large multifunctional prolease 2) protease 2) 23109 1072 D10854 N aido-keto reductase family 1, member A1 aldo-keto reductase family 1, member A1 8640 1073 D12769 D Kruppel-like factor 9 Kruppel-like factor 9 24428 1074 D13126 N neural visinin-like Ca2+-binding protein type 3 neural visinin-like Ca2+-binding protein type 3 15281 1075 D13623 N 25257 1075 D13623 N (nuclear receptor subfamily 1, group H, member 4, (nuclear receptor subfamily 1, group H, member 4, solute carrier family 2, 1214 1076 D13871 M,N,K solute carrier family 2, member 5) member 5) 18958 1077 D13921 N acetyl-coenzyme A acetyltransferae 1 acetyl-coenzyme A acetyltransferase 1 18727 1078 D13978 N argininosuccinate lyase argininosuccinate lyase 11434 1079 D14014 N,B cyclin D1 cyclin D1 19834 1080 D14048 E system N1 Na+ and H+-coupled glutamine transporter system N1 Na+ and H+-coupled glutamine transporter 18246 1081 D14441 N,B,F brain acidic membrane protein brain acidic membrane protein 503 1082 D16443 C prostaglandin E receptor 3 prostaglandin E receptor 3 hydroxyacyl-Coenzyme A dehydrogenase/3-ketoacyl- Coenzyme A hiolase/enoyl-Coenzyme A hydratase hydroxyacyl-Coenzyme A dehydrogenase/3-ketoacyl-Coenzyme A 16768 1083 D16478 N (trifunctional protein), alpha subunit hiolase/enoyl-Coenzyme A hydratase (trifunctional protein), alpha subunit 3015 1084 D16554 A polyubiquitin polyubiquitin 18452 1085 D17370 M,N CTL larget antigen CTL target antigen 18453 1085 D17370 N,G CTL larget antigen CTL target antigen Tyrosine 3-moncoxygenase/tryptophan 5- Tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, 16683 1086 D17445 N monooxygenase activation protein, eta polypeptide eta polypeptide Tyrosine 3-monooxygenase/tryptophan 5- Tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, 16684 1086 D17445 M monooxygenase activation protein, eta polypeptide eta polypeptide 13369 1087 D21132 D phosphotidylinositol transfer protein, beta phospholidylinositol transfer protein, beta 24885 1088 D25224 N laminin receptor 1 (67kD, ribosomal protein SA) laminin receptor 1 (67kD, ribosomal protein SA) 472 1089 D26111 G chloride channel K1-like chloride channel K1-like 20493 1090 D28339 M,N 3-hydroxyanthranilate 3,4-dioxygenase 3-hydroxyanthranilate 3,4-dioxygenase 16610 1091 D28557 N,E,L cold shock domain protein A cold shock domain protein A Tyrosine 3-monooxygenase/tryptophan 5- Tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, 25279 1092 D30740 C monooxygenase activation protein, zeta polypeptide zeta polypeptide Table 1 GLGC GenBank Acc or Model Identifier Seq ID RetSeq ID Code Known Gene Name UniGene Cluster Title 28 1093 D31662 M,F,G,I,J,L Regucalcin Regucalcin 187 1094 D32209 F acidic nuclear phosphoprotein 32 family, member A acidic nuclear phosphoprotein 32 family, member A 16681 1095 D37920 N,B,L squalene epoxidase squalene epoxidase human immunodeficiency virus type 1 enhancer- 24631 1096 D37951 F binding protein 2 human immunodeficiency virus type 1 enhancer-binding protein 2 5492 1097 D38061 N UDP glycosyltransferae 1 family, polypeptide A6 UDP glycosyltransferae 1 family, polypeptide A6 18028 1098 D38062 N UDP glycosyltransferae 1 family, polypeptide A7 UDP glycosyltransferae 1 family, polypeptide A7 1354 1099 D38065 N UDP glycosyltransferae 1 family, polypeptide A1 UDP glycosyltransferae 1 family, polypeptide A1 755 1100 D38448 M,N diacylglycerol kinase, gamma diacylglycerol kinase, gamma 16650 1101 D42137 E annexin 5 annexin 5 25290 1102 D42148 N,J growth arrest specific 6 growth arrest specific 6 20494 1103 D44494 N,E 3-hydroxyanthranilate 3,4-dioxygenase 3-hydroxyanthranilate 3,4-dioxygenase 20801 1104 D44495 M,N,H,I,J,L apurinic/apyrimidinic endonuclease 1 apurinic/apyrimidinic endonuclease 1 18750 1105 D45250 N,G protease (prosome, macropain) 28 subunit, beta protease (prosome, macropain) 28 subunit, beta 20960 1106 D45254 D cellular nucleic acid binding protein cellular nucleic acid binding protein 245 1107 D45412 J protein tyrosine phosphatase, receptor type, O protein tyrosine phosphatase, receptor type, O 16354 1108 D50564 N,C mercaptopyruvate sulfurtransferase mercaptopyruvate sulfurtransferase proteasome (prosome, macropain) 26S subunit, 1884 1109 D50695 I ATPase, 4 proteasome (prosome, macropain) 26S subunit, ATPase, 4 811 1110 D63704 M,I dihydropyrimidinase dihydropyrimidinase 812 1110 D63704 M,I dihydropyrimidinase dihydropyrimidinase 21147 1111 D63772 M,F,H,I,J,L solute carrier family 1, member 1 solute carrier family 1, member 1 770 1112 D83044 M,N solute carrier family 22, member 2 solute carrier family 22, member 2 (UDP glycosyltransferase 1 family, polypeptide A1, UDP glycosyltransferase 1 family, polypeptide A6 UDP (UDP glycosyltransferase 1 family, polypeptide A1, UDP glycosyltransferase 1 glycosyltransferase 1 family, polypeptide A7, UDP- family, polypeptide A6, UDP glycosltransferase 1 family, polypeptide A7, 15126 1113 D83796 N glucuronosyltransferae 1A8) UDP-glucuronosyltransferase 1A8) 15437 1114 D84418 E high mobility group box 2 high mobility group box 2 solute carrier family 27 (fatty acid transporter), member 17554 1115 D85100 N 32 solute carrier family 27 (fatty acid transporter), member 32 Table 1 GLGC GenBank Acc or Model Identifier Seq ID RetSeq ID Code Known Gene Name UniGene Cluster Title 13005 1116 D85189 N,C fatty acid Coenzyme A ligase, long chain 4 fatty acid Coenzyme A ligase, long chain 4 16448 1117 D86297 N aminolevulinic acid synthase 2 aminolevulinic acid synthase 2 15297 1118 D86641 N,K (FK506 binding protein 2, FK506-binding protein 1a) (FK506 binding protein 2, FK506-binding protein 1a) 968 1119 D86745 G,K nuclear receptor subfamily 0, group B, member 2 nuclear receptor subfamily 0, group B, member 2 945 1120 D88666 N phosphatidylserine-specific phospholipase A1 phosphatidylserine-specific phospholipase A1 25315 1121 D89730 N proteasome (prosome, macropain) subunit, alpha type 3987 1122 D90258 M,N 3 proteasome (prosome, macropain) subunit, alpha type 3 1921 1123 E01524 N P450 (cytochrome) oxidoreductase P450 (cytochrome) oxidoreductase 25024 1124 E03229 N cytosolic cystein dioxygenase 1 cytosolic cysteine dioxygenase 1 19824 1125 E13557 N,G,K cystein-sulfinate decarboxylase cysteine-sulfinate decarboxylase Rattus norvegicus transcribed sequence with strong similarity to protein pirT14781 (H.sapiens) T14781 hypothetical protein DKFZp586B1621.1 - 4360 1126 H31813 M,G,I human (fragment) 4361 1127 H31839 N BCL2-antagonist/killer 1 BCL2-antagonist/killer 1 21011 1128 H32189 N glutathione S-transferase, mu 1 glutathione S-transferase, mu 1 4386 1129 H33093 N Rattus norvegicus transcribed sequences Rattus norvegicus transcribed sequence with moderale similarity to protein ref:NP_219480.1 (H.sapiens) hypothetical protein similar to CG7943 [Homo 24033 1130 H33101 H sapiens] 17159 1131 J00797 M,G,K alpha-tubulin alpha-tubulin 1301 1132 J02585 N stearoyl-Coenzyme A desaturase 1 stearoyl-Coenzyme A desaturase 1 21012 1133 J02592 N,B Glutathione-S-transferase, mu type 2 (Yb2) Glutathione-S-transferae, mu type 2 (Yb2) (UDP glycosyltransferase 1 family, polypeptide A1, UDP glycosyltransferase 1 family, polypeptide A6, UDP (UDP glycosyltransferase 1 family, polypeptide A1, UDP glycosyltransferase 1 glycosyltransferase 1 family, polypeptide A7, UDP- family, polypetide A6, UDP glycosyltransferase 1 family, polypeptide A7, 15124 1134 J02612 N,B glucuronosyltransferase 1A8) UDP-glucuronosyltransferase 1A8) eukaryotic translation initiation factor 2, subunit 1 (alpha 4592 1135 J02646 H ) eukaryotic translation initiation factor 2, subunit 1 (alpha) Cylochrome P450, subfamily IIC (mephenytoin 4- 1174 1136 J02657 N hydroxylase) Cytochrome P450, subfamily IIC (mephenytoin 4-hydroxylase) 1698 1137 J02679 M,B,H,I NAD(P)H dehydrogenase, quinone 1 NAD(P)H dehydrogenase, quinone 1 16080 1138 J02722 N Heme oxygenase Heme oxygenase Table 1 GLGC GenBank Acc or Model Identifier Seq ID RetSeq ID Code Known Gene Name UniGene Cluster Title acetyl-Coenzyme A acyltransferase 1 (peroxisomal 3- acetyl-Coenzyme A acyltransferase 1 (peroxisomal 3-oxoacyl-Coenzyme A 23698 1139 J02749 N,D oxoacyl-Coenzyme A thiolase) thiolase) acetyl-Coenzyme A acyltransferase 1 (peroxisomal 3- acetyl-Coenzyme A acyltransferase 1 (peroxisomal 3-oxoacyl-Coenzyme A 23699 1139 J02749 N,D,E oxoacyl-Coenzyme A thiolase) thiolase) 16148 1140 J02752 N acyl-coA oxidase acyl-coA oxidase 16476 1141 J02773 M,L fatty acid binding protein 3 fatty acid binding protein 3 1514 1142 J02780 N Tropomycin 4 Tropomycin 4 21078 1143 J02791 N,G acetyl-coenzyme A dehydrogenase, medium chain acetyl-coenzyme A dehydrogenase, medium chain 21013 1144 J02810 N glutathione S-transferase, mu 1 glutathione S-transferase, mu 1 branched chain keto acid dehydrogenase subunit E1, 17284 1145 J02827 N,G alpha polypeptide branched chain keto acid dehydrogenase subunit E1, alpha polypeptide branched chain keto acid dehydrogenase subunit E1, 17285 1145 J02827 N alpha polypeptide branched chain keto acid dehydrogenase subunit E1, alpha polypeptide 22321 1146 J02962 M,B,G,L lectin, galactose binding, soluble 3 lectin, galactose binding, soluble 3 1762 1147 J03179 N D site albumin promoter binding protein D site albumin promoter binding protein 1763 1147 J03179 N D site albumin promoter binding protein D site albumin promoter binding protein 21038 1148 J03190 H aminolevulinic acid synthase 1 aminolevulinic acid synthase 1 21039 1148 J03190 H aminolevulinic acid synthase 1 aminolevulinic acid synthase 1 13479 1149 J03481 N quinoid dihydropteridine reductase quinoid dihydropleridine reductase 13480 1149 J03481 N quinoid dihydropteridine reductase quinoid dihydropleridine reductase 14997 1150 J03572 N alkaline phosphatase, tissue-nonspecific alkaline phosphatase, tissue-nonspecific 16948 1151 J03588 N,A,C Guanidinoacetate methyltransferase Guanidinoacetate methyltransferase 19040 1152 J03627 M,C,G,K S100 calcium binding protein A10 (calpaclin) S100 calcium binding protein A10 (calpactin) 15017 1153 J03752 N,B microsomal glutathione S-transferase 1 microsomal glutathione S-transferase 1 24459 1154 J03886 C myosin light chain kinase 2, skeletal muscle myosin light chain kinase 2, skeletal muscle 21014 1155 J03914 B,L Glutathione-S-transferase, mu type 2 (Yb2) Glutathione-S-transferase, mu type 2 (Yb2) 17394 1156 J03969 M,N,L nucleophosmin 1 nucleophosmin 1 7784 1157 J04591 M,N,I Dipeptidyl peptidase 4 Dipeptidyl peptidase 4 23524 1158 J04792 N 17393 1159 J04943 M,N nucleophosmin 1 nucleophosmin 1 6780 1160 J05029 N acetyl-Coenzyme A dehydrogenase, long-chain acetyl-Coenzyme A dehydrogenase, long-chain 4450 1161 J05031 N,E Isovaleryl Coenzyme A dehydrogenase Isovaleryl Coenzyme A dehydrogenase 4451 1161 J05031 M,N,F Isovaleryl Coenzyme A dehydrogenase Isovaleryl Coenzyme A dehydrogenase Table 1 GLGC GenBank Acc or Model Identifier Seq ID RetSeq ID Code Known Gene Name UniGene Cluster Title (UDP glycosyltransferase 1 family, polypeptide A1, UDP glycosyltransferase 1 family, polypeptide A6, UDP (UDP glycosyltransferase 1 family, polypeptide A1, UDP glycosyltransferase 1 glycosyltransferase 1 family, polypeptide A7, UDP- family, polypeptide A6, UDP glycosyltransferase 1 family, polypeptide A7, 15125 1162 J05132 N,B glucuronosyltransferase 1A8) UDP-glucuronosyltransferase 1A8) 1247 1163 J05181 N,J glutamate-cysteine ligase catalytic subunit glutamate-cysteine ligase catalytic subunit 1977 1164 J05470 N,L Camitine palmitoyltransferase 2 Camitine palmitoyltransferase 2 10464 1165 J05510 M,I inositol 1,4,5-triphosphate receptor 1 inositol 1,4,5-triphosphate receptor 1 1549 1166 J05519 G C1-tetrahydrofolate synthase C1-tetrahydrofolate synthase 24563 1167 J05592 N,G,K protein phosphalase 1, regulatory (inhibitor) subunit 1A protein phosphatase 1, regulatory (inhibitor) subunit 1A 24564 1167 J05592 N,G,K protein phosphalase 1, regulatory (inhibitor) subunit 1A protein phosphatase 1, regulatory (inhibitor) subunit 1A 18989 1168 K00136 N glutathione-S-transferase, alpha type2 glutathione-S-transferase, alpha type2 11136 1169 K00750 J 11137 1169 K00750 J 634 1170 K01932 N glutathione S-transferase, alpha 1 glutathione S-transferase, alpha 1 1850 1171 K02814 M T-kininogen T-kininogen 20149 1172 K03243 N,F enoyl-Coenzyme A, hydratase/3-hydroxyacyl 17758 1173 K03249 N Coenzyme A dehydrogenase enoyl-Coenzyme A, hydratase/3-hydroxyacyl Coenzyme A dehydrogenase 10878 1174 K03250 N ribosomal protein S11 ribosomal protein S11 20865 1175 L00117 M,N Elastase 1 Elastase 1 1894 1176 L03201 N,B,L cathepsin S cathepsin S 1712 1177 L06096 M inositol 1, 4, 5-triphosphate receptor 3 inositol 1, 4, 5-triphosphate receptor 3 15411 1178 L07736 N,B,L camitine palomitoyltransferase 1 camitine palmitoyltransferase 1 617 1179 L08831 N Glucose-dependent insulinotropic peptide Glucose-dependent insulinotropic peptide 8984 1180 L10652 D methionine aminopeptidase 2 methionine aminopeptidase 2 3549 1181 L11319 N signal peptidase complex 18kD signal peptidase complex 18kD 574 1182 L13039 M,E,G,K calpactin I heavy chain calpactin I heavy chain 25364 1183 L13237 F 22412 1184 L13619 N,C,H growth response protein (CL-6) growth response protein (CL-6) 22413 1184 L13619 N,C,H growth response protein (CL-6) growth response protein (CL-6) 108 1185 L14002 J Polymeric immunoglobulin receptor Polymeric immunoglobulin receptor Table 1 GLGC GenBank Acc or Model Identifier Seq ID RetSeq ID Code Known Gene Name UniGene Cluster Title 25366 1186 L14003 J 109 1187 L14004 N Polymeric immunoglobulin receptor Polymeric immunogolbulin receptor 20414 1188 L14323 M Phospholipase C-beta1 Phospholipase C-beta1 2079 1189 L14462 F amino-terminal enhancer of split amino-terminal enhancer of split 1475 1190 L16764 N,C heat shock 70kD protein 1A heat shock 70kD protein 1A 24770 1191 L19031 M,N,G,I,J solute carrier family 21, member 1 solute carrier family 21, member 1 sulfotransferase family 1A, phenol-preferring, member 4748 1192 L19998 N 1 sulfotransferase family 1A, phenol-preferring, member 1 sulfotransferase family 1A, phenol-preferring, member 4749 1192 L19998 N 1 sulfotransferase family 1A, phenol-preferring, member 1 inhibitor of DNA binding 1, helix-loop-helix protein 10248 1193 L23148 N (splice variation) Inhibitor of DNA binding 1, helix-loop-helix protein (splice variation) 43 1194 L23413 N solute carrier family 26 (sulfate transporter), member 1 solute carrier family 26 (sulfate transporter), member 1 25377 1195 L25387 D phosphofructokinase, platelet 17401 1196 l25785 M,B,G Transforming growth factor beta stimulated clone 22 Transforming growth factor beta stimulated clone 22 19 1197 L26268 M B-cell translocation gene 1 B-cell translocation gene 1 22411 1198 L26292 N Kruppel-like factor 4 (gut) Kruppel-like factor 4 (gut) 22411 1198 L26292 M,C Kruppel-like factor 4 (gut) Kruppel-like factor 4 (gut) 605 1199 L27340 C sonic hedgehog homolog (Drosophila) sonic hedgehog homolog (Drosophila) 24219 1200 L27843 M,L protein tyrosine phosphatase 4a1 protein tyrosine phosphatase 4a1 15872 1201 L28135 N solute carrier family 2, member 2 solute carrier family 2, member 2 20458 1202 L31394 M,I,K,L parathyroid hormone receptor parathyroid hormone receptor 353 1203 L32591 M,H,I, growth arrest and DNA-damage-inducible 45 alpha growth arrest and DNA-damage-inducible 45 alpha 354 1203 L32591 M,H,I, growth arrest and DNA-damage-inducible 45 alpha growth arrest and DNA-damage-inducible 45 alpha 16520 1204 L33869 M,B,C,L ceruloplasmin ceruloplasmin 15111 1205 L34049 M,I low density lipoprotein receptor-related protein 2 low density lipoprotein receptor-related protein 2 15112 1205 L34049 M,I low density lipoprotein receptor-related protein 2 low density lipoprotein receptor-related protein 2 1321 1206 L37333 N glucose-6-phosphatase, catalytic glucose-6-phosphatase, catalytic 13682 1207 L38482 N 6405 1208 L38615 G glutathione synthetase glutathione synthetase 6406 1208 L38615 G glutathione synthetase glutathione synthetase 1427 1209 L38644 N karyopherin, beta 1 karyopherin, beta 1 18629 1210 L40362 G RT1 class lb gene RT1 class lb gene Table 1 GLGC GenBank Acc or Model Identifier Seq ID RetSeq ID Code Known Gene Name UniGene Cluster Title 24568 1211 L48060 M,B Known Gene Name UniGene Cluster Title 11955 1212 L48209 N cytochrome c oxidase, subunit VIII cytochrome c oxidase, subunit VIIIa 1920 1213 M10068 N P450 (cytochrome) oxidoreductase P450 (cytochrome) oxidoreductase 15741 1214 M11670 N Catalase Catalase 15189 1215 M11794 N,B Metallothionein Metallothionein 17765 1216 M11942 N heat shock protein 8 heat shock protein 8 17502 1217 M12156 N helerogeneous nuclear ribonucleoprotein A1 heterogeneous nuclear ribonucleoprotein A1 6055 1218 M12337 M,N,D Phenylalanine hydroxylase Phenylalanine hydroxylase 4254 1219 M12450 N Group-specific component (vitamin D-binding protein) Group-specific component (vitamin D-binding protein 7064 1220 M12919 N aldolase A aldolase A 25399 1221 M13010 F 1466 1222 M14050 N heat shock 70kD protein 5 heat shock 70kD protein 5 23651 1223 M14656 M,G,K secreted phosphoprotein 1 secreted phosphoprotein 1 20714 1224 M14972 J,L 455 1225 M15474 N,E tropomyosin 1, alpha tropomyosin 1, alpha 21053 1226 M15481 M insulin-like growth factor 1 insulin-like growth factor 1 19255 1227 M15562 N Rat MHC class II RT1.u-D-alpha chain mRNA, 3' end 19256 1227 M15562 N Rat MHC class II RT1.u-D-alpha chain mRNA, 3' end 17154 1228 M15883 J clathrin, light polypeptide (Lcb) clathrin, light polypeptide (Lcb) 20809 1229 M17069 N,D Calmodulin 2 (phosphorylase kinase, delta) Calmodulin 2 (phosphorylase kinase, delta) 25405 1230 M18330 N protein kinase, C, delta protein kinase C, delta 23872 1231 M18416 M early growth response 1 early growth response 1 17274 1232 M18854 J Rat T-cell receptor active beta-chain C-region mRNA, partial cds, clone TRB4 23806 1233 M19257 D Retinol-binding protein 1 Retinol-binding protein 1 24567 1234 M19304 N,F prolaclin receptor prolactin receptor 17197 1235 M19647 N 17198 1235 M19647 N,G kallikrein 1 kallikrein 1 25415 1236 M19648 G 4010 1237 M20131 N 20876 1238 M21060 J superoxide dismutase 1 superoxide dismulase 1 24437 1239 M22357 A Myelin-associated glycoprotein Myelin-associated glycoprotein Table 1 GLGC GenBank Acc or Model Identifier Seq ID RetSeq ID Code Known Gene Name UniGene Cluster Title 20481 1240 M22631 M,N,G,K Propionyl Coenzyme A carboxylase, alpha polypeptide Propionyl Coenzyme A carboxylase, alpha polypeptide 25419 1241 M22922 G 46 1242 M23697 N Plasminogen activator, tissue Plasminogen activator, tissue 15540 1243 M24067 K serine (or cysteine) proteinase inhibitor, member 1 serine (or cysteine) proteinase inhibitor, member 1 18619 1244 AM24324 N RT1 class lb gene RT1 class lb gene 11454 1245 M24604 M Proliferaling cell nuclear antigen Proliferating cell nuclear antigen 11455 1245 M24604 M Proliferaling cell nuclear antigen Proliferating cell nuclear antigen 1540 1246 M25073 N alanyl (membrane) aminopeptidase alanyl (membrane) aminopeptidase M,N,A,B,H, 17541 1247 M26125 I epoxide hydrolase 1 epoxide hydrolase 1 16245 1248 M26534 G 23225 1249 M27467 N cytochrome oxidase subunit VIC cytochrome oxidase subunit VIc 11956 1250 M28255 N cytochrome c oxidase, subunit VIIIa cytochrome c oxidase, subunit VIIIa 17104 1251 M29358 M,G ribosomal protein S6 ribosomal protein S6 17105 1251 M29358 N ribosomal protein S6 ribosomal protein S6 UDP-glcuronosyltransferase 2B3 precursor, 14346 1252 M31109 N,B,H microsomal UDP-glucuronosyltransferase 2B3 precursor, microsomal 1814 1253 M31174 N thyroid hormone receptor alpha throid hormone receptor alpha 18501 1254 M31178 N calbindin 1 calbindin 1 18502 1254 M31178 N calbindin 1 calbindin 1 1312 1255 M31788 J phosphglycerale kinase 1 phosphoglycerate kinase 1 20868 1256 M32062 N Fc receptor, IgG, low affinity III Fc receptor, IgG, low affinity III 20869 1256 M32062 N Fc receptor, IgG, low affinity III Fc receptor, IgG, low affinity III 20298 1257 M32783 N,I 15580 1258 M33648 N 3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2 3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2 11755 1259 M33746 N,B,H UDP-glucuronosyltransferase 2 family, member 5 UDP-glucuronosyltransferase 2 family, member 5 35 1260 M33822 C gamma-glutamyl transpeplidase gamma-glutamyl transpeptidase 1844 1261 M33962 J protein tyrosine phosphatase, non-receptor type 1 protein tyrosine phosphatase, non-receptor type 1 24672 1262 M34097 C granzyme B granzyme B 20126 1263 M34253 N,K interferon regulatory factor 1 Interferon regulatory factor 1 24590 1264 M35299 N,D serine protease inhibitor, Kazal type 1 serine protease inhibitor, Kazal type 1 20699 1265 M35601 N Fibrinogen, A alpha polypeptide Fibrinogen, A alpha polypeptide Table 1 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Known Gene Nam UniGene Cluster Title 20700 1265 M35601 N Fibrinogen, A alpha polypeptide Fibrinogen, A alpha polypeplide 21400 1266 M36410 c.F sepiaplerin reductast sepiapterin reductase 17661 1267 M37584 N,E H2A histone family, member Z H2A histone family, member Z 67 1268 M37828 B cylochrome P450, 4a12 cytochrome P450, 4a12 9109 1269 M38135 N Cathepsin H Cathepsin H 17807 1270 M54926 M,G lactate dehydrogenase A lactate dehydrogenase A 8829 1271 M55015 M,A,F,K Nucleolin Nucleolin 13723 1272 M55534 N,K crystallin, alpha B crystallin, alpha B 1246 1273 M57507 M,J guanylate cyclase, soluble, beta 2 guanylate cyclase, soluble, beta 2 4467 1274 M57664 N creatine kinase, brain creatine kinase, brain 20713 1275 M57718 N,J,L cytochrome P450,4A1 cytochrome P450,4A1 20816 1276 M58404 M,G,K thymosin, beta 10 thymosin, beta 10 25057 1277 M58495 N 16982 1278 M58634 M,B,L insulin-like growth factor binding protein 1 insulin-like growth factor binding protein 1 ATPase, H+ transporting, lysosomal noncatalylic 20641 1279 M58758 H accessory protein 1a ATPase, H+ transporting, lysosomal noncatalytic accessory protein 1a 2465 1280 M59814 G,K Eph receptor B2 Eph receptor B2 12606 1281 M59861 N,E,K 10-formyltetrahydrololate dehydrogenase 10-formyltetrahydrololate dehydrogenase 457 1282 M60666 E,G,K tropomyosin 1, alpha tropomyosin 1, alpha 15300 1283 M60921 M B-cell transiocation gene 2 B-cell translocation gene 2 17378 1284 M62388 N,D ubiquitin conjugating enzyme ubiquitin conjugating enzyme 24431 1285 M63282 M,F Activating transcription factor 3 Activating transcription factor 3 14956 1286 M64301 N mitogen-activated protein kinase 6 mitogen-activated protein kinase 6 14957 1286 M64301 N milogen-activated prolein kinase 6 mitogen-activated protein kinase 6 7101 1287 M64733 M,E clusterin clusterin 19825 1288 M64755 N cysteine-sulfinate decarboxylase cysteine-sulfinate decarboxylase 19110 1289 M64986 A.J high mobility group box 1 high mobility group box 1 21663 1290 M65149 M,C,I,L CCAAT/enhancerbinding, protein (C/EBP) delta CCAAT/enhancerbinding, protein (C/EBP) delta 21193 1291 M69055 F Insulin-like growth factor binding protein 6 serine (or cysteine) proteinase inhibitor, clade H, 17301 1292 M69246 N,E,I member 1 serine (or cysteine) proteinase inhibitor, clade H, member 1 23884 1293 M73714 J aldehyde dehydrogenase family 3, subfamily A2 aldehyde dehydrogenase family 3, subfamily A2 24648 1294 M74054 M,N angiotensin receptor 1a angiotensin receptor 1a Table 1 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Known Gene Nam UniGene Cluster Title 20405 1295 M74067 N,B claudin 3 claudin 3 24566 1296 M74152 B,F,L prolactin receptor protactin receptor 240 1297 M75153 N RAB11a, member RAS oncogene family RAB11a, member RAS oncogene family 23961 1298 M77694 M,N,E,G,I fumarylacetoacetate hydrolase fumarylacetoacetate hydrolase 1527 1299 M77850 B 6-pyruvoyl-tetrahydropeterin synthase 6-pyruvoyl-tetrahydroplerin synthase 1622 1300 M80804 N solute carrier family 3, member 1 solute carrier family 3, member 1 24843 1301 M80826 N,J trefoil factor 3 trefoil fator 3 1529 1302 M81687 M,B,F,I syndecan 2 syndecan 2 (ATP-binding cassette, sub-family B (MDR/TAP), (ATP-binding cassette, sub-family B (MDR/TAP), member 1A, p- 5733 1303 M81855 N member 1A, P-glycoprotein/muitidrug resistance 1) glycoprotein/multidrug resistance 1) 17149 1304 M83107 N Transgelin (Smooth muscle 22 protein) Transgelin (Smooth muscle 22 prolein) 17150 1304 M83107 N Transgelin (Smooth muscie 22 protein) Transgelin (Smooth muscle 22 protein) Sialyltransferase 1 (beta-galactoside alpha-2,6- 4198 1305 M83143 M,N,I sialytransferase) Sialyltransferase 1 (beta-galactoside alpha-2,6-sialytransferase) Sialyltransferase 1 (beta-galactoside alpha-2,6- 4199 1305 M83143 M,N sialytransferase) Sialyltransferase 1 (bela-galactoside alpha-2,6-sialytransferase) 24651 1306 M83678 N RAB13 RAB13 20831 1307 M83680 B GTPase Rab14 GTPase Rab14 6-pyruvoyl-tetrahydropterin synthase/dimerization 6-pyruvoyl-tetrahydroplerin synthase/dimerization cofactor of hepaiocyle 21882 1308 M83740 M,N,D cofactor of hepatocyte nuclear factor 1 alpha nuclear factor 1 alpha 1430 1309 M84648 M dopa decarboxylase dopa decarboxylase 23445 1310 M84719 M,N Flavin-containing monooxygenase 1 Flavin-containing monooxygenase 1 24438 1311 M85183 M,N,F,L angiolensin/vasopressin receptor angiolensin/vasopressin receptor 24496 1312 M85300 M,N,I,K solute carrier family 9, member 3 solute camier lamily 9, member 3 16895 1313 M86240 N fructose-1,6-biphosphatase 1 fructose-1,6-biphosphatase 1 17736 1314 M86389 H,K heat shock 27kDa prolein 1 heat shock 27kDa protein 1 7872 1315 M86912 M,N,B 25453 1315 M86912 M,L 291 1316 M88347 M,N,F Cystathionine beta synthase Cystathionine beta synthase 17357 1317 M88601 M,F,G,I,L Meprin 1 beta Meprin 1 beta 24615 1318 M89646 N,D ribosomal protein S24 ribosomal protein S24 15069 1319 M89945 H farensyl diphosphate synthase farensyl diphosphate synthase 25460 1319 M89945 N farensyl diphosphate synthase farensyl diphosphate synthase Table 1 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Known Gene Nam UniGene Cluster Title 11153 1320 M91652 N glutamine synthetase 1 glutamine synthelase 1 25467 1321 M93297 N,G ornithine aminotransferase cmithine aminotransferase 17269 1322 M93401 M methylmalonate semialdehyde dehydrogenase gene methylmalonate semialdehyde dehydrogenase gene cylochrome P450, subfamily IVF, polypeptide 14 cytochrome P450, subfamily IVF, polypeplide 14 (leukotriene B4 omega 20716 1323 M94548 G (leukotriene B4 omega hydroxylase) hydroxylase) 25468 1324 M94918 N,J hemoglobin beta chain complex hemoglobin beta chain complex 25469 1325 M94919 N,J 1976 1326 M95493 N guanylate cyclase activator 2A guanylate cyclase activator 2A 16449 1327 M95591 N farnesyl diphosphate famesyl transferase 1 famesyl diphosphate famesyl transferase 1 16450 1327 M95591 N farnesyl diphosphate famesyl transferase 1 famesyl diphosphate famesyl transferase 1 solute carrier family 6 (neurotransmitter transporter, 729 1328 M95762 N,D GABA),member 13 solute carrier family 6 (neurotransmitter transporter, GABA), member 13 25470 1329 M95791 E 1410 1330 M96548 H zinc finger protein 354A zinc finger protein 354A 1678 1331 M96674 N glucagon receptor glucagon receptor 1508 1332 M97662 N,G ureidopropionase, beta ureidopropionase, beta 22434 1333 NM_012974 F Laminin chan beta 2 Laminin chain beta 2 21145 1334 NM_013032 M,B solute carrier family 1, member 1 solute carrier family 1, member 1 23708 1335 NM_013113N ATPase Na+/K+ transporting beta 1 polypeptide ATPase Na+/K+ transprorting beta 1 polypeptide 754 1336 NM_013126 N diacylglycerol kinase, gamma diacylglycerol kinase, gamma 16967 1337 NM_013146 E Caldesmon 1 Caldesmon 1 1946 1338 NM_017061 F lysyl oxidase lysyloxidase 13938 1339 NM_017212 N microtubule-associated protein tau microtubule-associated protein tau 13939 1339 NM_017212 D microtubule-associated protein tau microtubule-associated protein tau 15299 1340 NM_017259 M,I,J B-cell translocation gene 2 B-cell transiocation gene 2 15666 1341 NM_017265 L 15667 1341 NM_017265 L 1729 1342 NM_019147 N,B jagged 1 jagged 1 1143 1343 NM_019280 A gap junction membrane channel protein alpha 5 gap junction membrane channel protein alpha 5 235 1344 NM_019347 C solute carrier family 14, member 2 solute carrier family 14, member 2 18716 1345 NM-020075 F eukaryotic initialion factor 5 (eIF-5) eukaryotic initiation factor 5 (eIF-5) 7690 1346 NM_022284 M melanoma antigen, family D, 1 melanoma antigen, family D, 1 22414 1347 NM_022392 H growth response protein (CL-6) growth response protein (CL-6) Table 1 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Known Gene Nam UniGene Cluster Title 21024 1348 NM_022599 M synaptojanin 2 binding protein synaptojanin 2 binding protein 15201 1349 NM_031093 N 18008 1350 NM_031588 N neuregulin 1 neuregulin 1 16003 1351 NM_031757 C matrix metalloproteinase 24 (membrane-inserted) matrix metalloproteinase 24 (membrane-inserted) M,N,E,G,H 16726 1352 NM_031855 J Ketohexokinase Ketohexokinase 25802 1353 NM_031969 G,K Calmodulin 1 (phosphorylase kinase, delta) Calmodulin 1 (phosphorylase kinase, delta) 1888 1354 NM_057130 B BH3 interacting domain 3 BH3 interacting domain 3 23033 1355 NM_080888 A,C,K BCL2/adenovirus E1B 19 kDa-interacting protein 3-like BCL2/adenovirus E1B 19 kDa-interacting protein 3-like (AT{ase Ma+K+ transporting beta 1 polypeptide, 23709 1356 NM_138532 N NME7) (ATPade Na+/K+ transporting beta 1 polypeptide, NME7) 15072 1357 NM_144730 A GATA-binding protein 4 GATA-binding protein 4 26083 1358 NM_147146 B,H 24232 1359 NM_171992 B cyclin D1 cyclin D1 20795 1360 NM_175761 N,H heat shock protein 86 heat shock protein 86 5952 1361 NM_181090 E solute carrier family 38, member 2 solute carrier family 38, member 2 (solute carrier family 7 (cationic amino acid transporter, y+ system), member 8, synaptic Ras GTPase activating (solute carrier family 7 (cationic amino acid transporter, y+ system), member 24762 1362 NM_181092 M,D protein 1) 8, synaplic Ras GTPase activating prolein 1) 5837 1363 S43408 M,N,F Meprin 1 alpha Meprin 1 alpha 5838 1363 S43408 M,F,G Meprin 1 alpha Meprin 1 alpha 25064 1364 S45392 N,H,K insulin-like growth factor binding protein, acid labile 21977 1365 S46785 A,B subunit insulin-like growth factor binding prolein, acid labile subunit insulin-like growth factor binding protein, acid labile 25480 1365 S46785 N subunit insulin-like growth lactor binding protein, acid labile subunit 25481 1366 S46798 N 4012 1367 S48325 N,J cytochrome P450, subfamily 2E, polypeptide 1 cylochrome P450, subfamily 2E, polypeptide 1 10886 1368 S49003 N 5493 1369 S56936 N UDP glycosyltransterase 1 family, polypeptide A6 UDP glycosyltransferase 1 family, polypeptide A6 Table 1 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Known Gene Nam UniGene Cluster Title (UDP glycosyltransferase 1 family, polypeptide A1, UDP glycosyltransferase 1 family, polypeptide A6, UDP (UDP glycosyltransterase 1 family, polypeptide A1, UDP glycosyltransferase 1 glycosyltransferase 1 family, polypeptide A7, UDP- family, polypeptide A6, UDP glycosyltransferase 1 family, polypeptide A7, 15127 1370 S56937 N glucuronosyltransferase 1A8) UDP-glucuronosyltransferase 1A8) 7196 1371 S57478 M,E,G,K annexin 1 annexin 1 8210 1372 S61960 M 3244 1373 S63519 M 14003 1374 S65555 N,B,J glutamate cysteine ligase, modifier subunit glutamate cysteine ligase, modifier subunit 355 1375 S66024 N cAMP responsive element modulator cAMP responsive element modulator 356 1375 S66024 N cAMP responsive element modulator cAMP responsive element modulator 16248 1376 S68135 N solute carrier family 2,member 1 solute carrier family 2,member 1 15832 1377 S68589 N 1471 1378 S68809 N S100 calcium binding protein A1 18647 1379 S69316 N tumor rejection antigen gp96 20740 1380 S69874 D fatty acid binding prolein 5, epidermal fatty acid binding protein 5, epidermal 9224 1381 S70011 N,C 25518 1381 S70011 N 15135 1382 S71021 N,G ribosomal protein L6 ribosomal prolein L6 25525 1383 S72505 N glutathione S-transferase, alpha 1 glutathione S-transferase, alpha 1 18990 1384 S72506 N,H 15137 1385 S73424 L macrophage migration inhibitory factor macrophage migration inhibitory factor 16211 1386 S75960 N uromodulin uromodulin 1460 1387 S76054 M,A,C,I,K 1943 1388 S77494 N,L lysyl oxidase lysyl oxidase 21583 1389 S77900 N 25545 1389 S77900 N 25546 1390 S78154 N,K 25547 1391 S78556 C 25550 1392 S79213 J protein phosphatase 1, regulatory (inhibitor) subunit 2 10260 1393 S81497 N lipase A, lysosomal acid lipase A. lysosomal acid 25563 1393 S81497 N lipase A, lysosomal acid lipase A, lysosomal acid 14121 1394 S82383 N,I tropomyosin isoform 6 tropomyosin isoform 6 3609 1395 S82579 N,F histamine N-methyltransferase histamine N-methyltransferase Table 1 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Known Gene Nam UniGene Cluster Title 25069 1396 S82820 N,H 25070 1397 S83279 M,N peroxisomal multifunctional enzyme type II peroxisomal multifunctional enzyme type II 3430 1398 S85184 M,G,I 25567 1398 S85184 M,I ATP synthase, H+ transporting, mitochondrial F1 18449 1399 U00926 H complex, delta subunit ATP synthase, H+ transporting, mitochondrial F1 complex, delta subunit 347 1400 U01914 D A kinase anchor protein 8 A kinase anchor protein 8 18005 1401 U02320 N neuregulin 1 neuregulin 1 18011 1402 U02322 M,H neuregulin 1 neuregulin 1 20885 1403 U04842 N,G,K epidermal growth factor epidermal growth factor eukaryotic translation initiation factor 4E binding protein 1570 1404 U05014 A 1 eukaryotic translation initiation factor 4E binding protein 1 2010 1405 U05675 K Fibrinogen, B beta polypeptide Fibrinogen, B beta polypeptide 23606 1406 U05784 N microtubule-associated proteins 1A/1B light chain 3 microlubule-associated proteins 1A/1B light chain 3 17806 1407 U06273 N UDP-glucuronosyltransferase UDP-glucuronosyltransferase 17805 1408 U06274 N,B UDP-glucuronosyltransferase UDP-glucuronosyltransferase 7124 1409 U07181 E lactate dehydrogenase B lactate dehydrogenase B 24874 1410 U07619 N coagulation factor 3 coagulation factor 3 glycine amidinotransferase (L-arginine:glycine 16775 1411 U07971 M,D,I,L amidinotransferase) glycine amidinotransferase (L-arginine:glycine amidinotransferase) 20925 1412 U08976 N,L enoyl coenzyme A hydratase 1 enoyl coenzyme A hydratase 1 20803 1413 U09256 N,B,H,I transketolase transketolase 4532 1414 U10096 J solute carrier family 12, member 1 solute carrier family 12, member 1 646 1415 U10097 N,G,K solute carrier family 12, member 3 solute carrier family 12, member 3 solute carrier family 28 (sodium-coupled nucleoside 714 1416 U10279 N transporter), member 1 solute carrier family 28 (sodium-coupled nucleoside transporter), member 1 45 1417 U10354 M,J,L calcium-sensing receptor calcium-sensing receptor 1928 1418 U10357 N pyruvate dehydrogenase kinase 2 pyruvate dehydrogenase kinase 2 1929 1418 U10357 N,A,C,D,E pyruvate dehydrogenase kinase 2 pyruvate dehydrogenase kinase 2 (allograft inflammalory factor 1, balloon angioplasly 16268 1419 U10894 N responsive transcript) (allograft inflammatory factor 1, balloon angioplasty responsive transcript) 24900 1420 U12973 N,H X transprorter protein 2 X transporter protein 2 Table 1 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Known Gene Nam UniGene Cluster Title ubiquitin-conjugating enzyme E2D 3 (homologous to 15273 1421 U13177 E yeast UBC4/5) ubiquilin-conjugating enzyme E2D 3 (homologous to yeast UBC4/5) 20443 1422 u14192 H vesicle docking protein, 115 kDa vesicle docking protein, 115 kDa 1424 1423 U14746 N von Hippel-Lindau syndrome homolog von Hippel-Lindau syndrome homolog 809 1424 U17035 C chemokine (C-X-C motif) ligand 10 chemokine (C-X-C motif) ligand 10 mini chromosome maintenance deficient 6 (S. 16674 1425 U17565 E cerevisiae) mini chromosome maintenance deficient 6 (S. cerevisiae) mini chormosome maintenance deficient 6 (S. 16675 1425 U17565 N,E cerevisiae) mini chromosome maintenance deficient 6 (S. cerevisiae) 9520 1426 U17837 B 1824 1427 U17971 K protein tyrosine phosphatase 2E protein tyrosine phosphatase 2E 16871 1428 U18314 N,E thymopoietin thymopoielin 19712 1429 U18374 K nuclear receptor subfamily 1, group H, member 4 nuclear receptor subfamily 1, group H, member 4 17999 1430 U19485 M spp-24 precursor spp-24 precursor 18000 1430 U19485 1 spp-24 precursor spp-24 precursor 1949 1431 U19614 A lamina-associated polypeptide 1C lamina-associated polypeptide 1C 25589 1432 U21718 F hypothetical RNA binding protein RDA288 hypothetical RNA binding protein RDA288 Rattus norvegicus clons D920 intestinal epithelium proliferating cell- 22196 1433 U21719 M,N associated mRNA sequence 275 1434 U22424 M hydroxysteroid 11-beta dehydrogenase 2 hydroxysteroid 11-beta dehydrogenase 2 1581 1435 U23769 M,A,C PDZ and LIM domain 1 PDZ and LIM domain 1 133 1436 U24174 N cyclin-dependent kinase inhibitor 1H cyclin-dependent kinase inhibitor 1A 1340 1437 U25651 B phosphofructokinase, muscle phosphofructokinase, muscie 1553 1438 U25808 J Kidney androgen-regulated protein Kindney androgen-regulated protein 200555 1439 U26033 F camitine O-octanoyltransferase camitine O-octanoyltransferase 1472 1440 U26356 K 1537 1441 U27516 N,H UDP-glucuronosyltransferase UDP-glucuronosyltransferase solute carrier family 17 vesicular glutamate transporter), 1558 1442 U28504 N,H member 1 solute carrier family 17 vesicular glutamate transporter), member 1 solute carrier family 17 vesicular glutamate transporter), 1559 1442 U28504 N member 1 solute carrier family 17 vesicular glutamate transporter), member 1 solute carrier family 17 vesicular glutamate transporter), 1559 1442 U28504 N member 1 solute carrier family 17 vesicular glutamate transporter), member 1 247 1443 u28938 J protein tyrosine phosphatase, receptor type, O protein tyrosine phosphatase, receptor type, O Table 1 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Known Gene Nam UniGene Cluster Title 20780 1444 U29881 M,N,D low affinity Na-dependent glucose transporter (SGLT2) low affinity Na-dependent glucose transporter (SGLT2) 1598 1445 U30186 N DNA-damage inducible transcript 3 DNA-damage inducible transcript 3 1970 1446 U31463 N,K myosin, heavy polypeptide 9 myosin, heavy polypeptide 9 1478 1447 U32314 M Pyruvale carboxylase Pyruvate carboxylase 1479 1447 U32314 N,D Pyruvale carboxylase Pyruvate carboxylase 18301 1448 U33500 M Raltus norvegicus retinol dehydrogenase type II mRNA, complete cds 18302 1448 U33500 M Rattus norvegicus retinol dehydrogenase type II mRNA, complete cds 16552 1449 U36482 L endoplasmic retucium prolein 29 endopiasmic reluclum protein 29 433 1450 U37142 C Brevican Brevican 23826 1451 U38180 N solute carrier family 19, member 1 solute carrier family 19, member 1 eukaryotic translation initiation factor 2B, subunit 3 797 1452 U38253 N (gamma, 58kD) eukaryotic translation initiation factor 2B, subunit 3 (gamma, 58kD) 15851 1453 U42719 M complement component 4a complement component 4a 24484 1454 U42967 H cholinergic receptor, nicotinic, beta polypeptide 4 cholinergic receptor, nicotinic, beta polypeptide 4 19543 1455 U44948 N cysteine rich protein 2 cysteine rich protein 2 1453 1456 U48596 F,K mitogen activated protein kinase kinase kinase 1 milogen activated protein kinase kinase kinase 1 1454 1456 U48596 M,K mitogen activated protein kinase kinase kinase 1mitogen activated protein kinase kinase kinase 1 20829 1457 U49062 M,D CD24 antigen CD24 anligen 20830 1457 U49062 M CD24 antigen CD24 antigen 15489 1458 U50194 F tripeptidylpeptidase II tripeptidylpeptidase II 16147 1459 U51898 M,N phospholipase A2, group VI phospholipase A2, group VI 21654 1460 U53184 M,I,L LPS-induced TNF-alpha factor LPS-induced TNF-alpha factor 25606 1461 U53214 C tubulin tyrosine ligase tubulin tyrosine ligase 12014 1462 U54632 N Ubiquitin conjugating enzyme E2I Ubiquitin conjugating enzyme E2I serine (or cysteine) proteinase inhibitor, clade A (alpha- serine (or cysteine) proteinase inhibitor, dade A (alpha-1 antiproteinase, 699 1463 U55765 E 1 antiproteinase, antitrypsin), member 10 antitrypsin), member 10 v-maf musculoaponeurotic fibrosarcoma (avian) 989 1464 U56242 N,D,F oncogene homolog (c-maf) v-mafmusculoaponeurotic fibrosarcoma (avian) oncogene homolog (c-maf) 16708 1465 U57042 M,N adenosine kinase adenosine kinase 15470 1466 U57050 H 26S proteasome, subunit p112 26S proteasome, subunit p112 1439 1467 U57391 H SH2-B PH domain containing signaling mediator 1 SH2-B PH domain containing signaling mediator 1 912 1468 U59184 N bcl2-associated X prolein bcl2-associated X protein Table 1 GLGC GenBank Acc or Moder Identifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Title 15174 1469 U59809 N insulin-like growth factor 2 receptor insulin-like growth factor 2 receptor heterogeneous nuclear riboucleoproteins heterogeneous nuclear ribonucleoproteins methyltransferase-like 2 (S. 20772 1470 U60882 N methyltransferase-like 2 (S. cerevisiae) cerevisiae) 725 1471 U62316 B solute carrier family 16, member 7 solute carrier family 16, member 7 15035 1472 U62897 B carboxypeptidase D carboxypeptidase D 1490 1473 U63839 E nucleoporin p58 nucleoporin p58 24234 1474 U63923 M,A,I thioredoxin reductase 1 thioredoxin reductase 1 20896 1475 U64030 A,F Deoxyuridinetriphosphatase (dUTPase) Deoxyuridinetriphosphatase (dUTPase) 794 1476 U68168 M,I kynureninae (L-kynurenine hydrolase) kynureninase (L-kynurenine hydrolase) 24643 1477 U68417 N,K branched chain aminotransferase, 2, milochondrial branched chain aminotransferase 2, milochondrial 16398 1478 U75392 N B-cell receptor-associated protein 37 B-cell receptor-associated protein 37 23869 1479 U75397 L early growth response 1 early growth response 1 2153 1480 U75404 M,L Rattus norvegicus Ssecks 322 mRNA, 3' untranslated region, partial sequence 25632 1481 U75405 N collagen, type 1, alpha 1 collagen, type 1, alpha 1 20682 1482 U75917 B clathrin-associated protein 17 clathrin-associated protein 17 1602 1483 U76379 N solute carrier family 22, member 1 solute carrier family 22, member 1 20886 1484 U76635 E,G Deoxyribonuclease I Deoxyribonuclease I 20887 1484 U76635 E,G Deoxyribonuclease I Deoxyribonuclease I solute carrier family 39 (iron-regulated transporter), 4956 1485 U76714 H member 1 solute carrier family 39 (iron-regulated transporter), member 1 solute carrier family 39 (iron-regulated transporter), 4957 1485 U76714 H member 1 solute carrier family 39 (iron-regulated transporter), member 1 25643 1486 U77829 N,A growth arrest specific 5 growth arrest specific 5 25647 1487 U83119 F 23300 1488 U84727 N 2-oxoglutarate carrier 2-oxoglutarate carrier 1546 1489 U85512 M,N,G GTP cyclohydrolase I feedback regulatory portein GTP cyclohydrolase I feedback regulatory protein M,A,H,I,K, 15032 1490 U89905 L alpha-methylacyl-CoA rancemase alpha-methylacyl-CoA racemase 23282 1491 U90725 A lipoprotein-binding protein lipoprotein-binding protein 1419 1492 U90887 N arginase 2 arginase 2 22675 1493 U92081 N,G glycoprotein 38 glycoprotein 38 1401 1494 U93692 J preimplantation protein 2 preimplantation protein 2 Table 1 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Title disabled homolog 2, mitogen-responsive 4504 1495 U951748D phosphoprotein (Drosophila) disabled homolog 2, mitogen-responsive phosphoprotein (Drosophila) 17158 1496 V01227 N alpha-tubulin alpha-tubulin 818 1497 X02291 N aldolase B aldolase B (glutathione S-transferase, pi 2, glutathione-S- 20818 1498 X02904 M,N transferase, pi 1) (glutathione S-transferase, pi 2, glutathione-S-transferase, pi 1) 14633 1499 X03478 H UDP glycosyltransferase 2 family, polypeptide B UDP glycosyltransferase 2 family, polypeptide B 33 1500 X03518 N gamma-glutamyl transpeptidase gamma-glutamyl transpeptidase 25662 1501 X05472 F 20849 1502 X05566 M,G,K moysin regulatory light chain myosin regulatory light chain 20513 1503 X05684 N pyruvate kinase, liver and RBC pyruvate kinase, liver and RBC 1550 1504 X06150 N Glycine methyltransferase Glycine methyltransferase 1551 1504 X06150 N,G Glycine methyltransferase Glycine methyltransferase 16204 1505 X06423 M,N,G ribosomal protein S8 ribosomal protein S8 16205 1505 X06423 N,F ribosomal protein S8 ribosomal protein S8 6577 1506 X06942 F A-raf A-raf 20715 1507 X07259 N,L cytochrome P450,4A1 cytochrome P450,4A1 1399 1508 X07467 M,H,I glucose-6-phosphate dehydrogenase glucose-6-phosphate dehydrogenase 23523 1509 X07944 N ornithine decarboxylase 1 ornithine decarboxylase 1 16947 1510 X08056 N Guanidinoacetate methyltransferase Guanidinoacetate methyltransferase 1853 1511 X12367 N Glutathione peroxidase 1 20597 1512 X12459 N arginosuccinate synthetase arginosuccinate synthetase 20884 1513 X12748 N,G,K epidermal growth factor epidermal growth factor 17377 1514 X13058 N tumor protein p53 tumor protein p53 24778 1515 X13119 N serine dehydratase serine dehydratase 16847 1516 X13549 N ribosomal protein S10 ribosomal protein S10 20810 1517 X14181 N,G 25675 1517 X14181 N 15653 1518 X14210 N,G ribosomal protein S4, X-linked 25676 1519 X14254 N 20518 1520 X14265 N calmodulin 3 calmodulin 3 19244 1521 X15013 N 1069 1522 X15096 N acidic ribosomal protein P0 acidic ribosomal protein P0 Table 1 GLGC GenBank Acc or Vodel dentifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Title 20167 1523 X15705 E testis-specific heat shock prolein-related gene hat70 testis-specific heat shock protein-realted gene hst70 20483 1524 X15939 N myosin heavy chain, polypeptide 7 moysin heavy chain, polypeptide 7 21562 1525 X15958 N,A enoyl Coenzyme A hydratase, short chain 1 enoyl Coenzyme A hydratase, short chain 1 14996 1526 X16038 M,D alkaline phosphatase, tissue-nonspecific alkaline phosphatase, tissue-nonspecific Protein phosphatase 2 (formerly 2A), catalystic subunit 3202 1527 X16043 N alpha isoform Protein phosphatase 2 (formerly 2A), catalytic subunit, alpha isoform 24582 1528 X16554 D phosphoribosyl pyrochosphate synthetase 1 phosphoribosyl prophosphate synthetase 1 1847 1529 X16555 B phosphoribosyl pyrophosphate synthetase 2 phosphoribosyl pyrophosphate synthetase 2 25682 1530 X16933 N RNA binding protein p45AUF1 RNA binding protein p45AUF1 20449 1531 X17053 M small inducible cylokine A2 small inducible cylokine A2 25686 1532 X51536 N,F ribosomal protein S3 23987 1533 X51615 N,B 20872 1534 X51707 N ribosomal protein S19 9620 1535 X53377 N ribosomal protein S7 ribosomal protein S7 20427 1536 X53378 N ribosomal protein S13 ribosomal protein S13 18606 1537 X53504 M 25691 1537 X53504 N,G 12903 1538 X53517 N CD37 antigen CD37 antigen 20617 1539 X53581 F 25692 1539 X53581 D 1463 1540 X54467 M,G,K cathepsin D cathepsin D ATP synthase, H+ transporting, mitochondrial F0 20725 1541 X54510 A complex, subunit F6 ATP synthase, H+ transporting, mitochondrial F0 complex, subunit F6 20848 1542 X54617 M,G,K 20161 1543 X54686 M,C,I jun B proto-oncogene jun B proto-oncogene 21575 1544 X55298 J ribophorin 2 ribophorin 2 proteasome (prosome, macropain) subunit, alpha type 1447 1545 X55986 D 4 proteasome (prosome, macropain) subunit, alpha type 4 21122 1546 X56228 N,E thiosulfate sulfurtransferase thiosulfate sulfurtransferase 21123 1546 X56228 N,D thiosulfate sulfurtransferase thiosulfate sulfurtransferase 1684 1547 X56325 J hemoglobin, alpha 1 hemoglobin, alpha 1 1885 1548 X56546 M,N transcription factor 2 transcription factor 2 10860 1549 X57133 N hepatocyte nuclear factor 4, alpha hepatocyte nuclear factor 4, alpha Table 1 GLGC GenBank Acc or Model Identifier Seq ID RelSeq ID Code Known Gene Name UniGene Cluster Title 25699 1549 X57133 N hepatoycte nuclear factor 4, alpha hepatocyte nuclear factor 4, alpha 10267 1550 X57432 N ribosomal protein S2 ribosomal protein S2 transporter 1, ATP-binding cassette, sub-family B 1037 1551 X57523 N (MDR/TAP) transporter 1, ATP-binding cassetle, sub-family B (MDR/TAP) 19678 1552 X57999 M deiodinase, iodothyronine, type I deiodinase, iodothyronine, type I 5667 1553 X58200 N ribosomal protein L23 18611 1553 X58200 N ribosomal protein L23 17175 1554 X58389 M,N 10109 1555 X58465 N,G ribosomal protein S5 25702 1555 X58465 N,G ribosomal protein S5 25705 1556 X59375 M,J 1141 1557 X59601 M,C,G plectin plectin 25707 1558 X59677 N solute carrier family 13, member 2 solute carrier family 13, member 2 18354 1559 X59859 J decorin decorin 21651 1560 X60767 N,E cell division cycle 2 homolog A (S, pombe) cell division cycle 2 homolog A (S. pombe) 21239 1561 X60769 M,H,I CCAAT/enhancer binding protein (C/EBP), beta CCAAT/enhancer binding protein (C/EBP), beta 21657 1562 X61381 M 15875 1563 X62145 N ribosomal protein L8 25718 1563 X62145 M,G ribosomal protein L8 4441 1564 X62146 N,G 25719 1564 X62146 N 13646 1565 X62166 M,N,A,G 18108 1566 X62528 N ribonuclease/angiogenin inhibitor ribonuclease/angiogenin inhibitor 16012 1567 X62875 M,I high mobility group At-hook 1 high mobility group AT-hook 1 15185 1568 X62952 M vimentin vimentin 556 1569 X64336 M,N Protein C Protein C 20844 1570 X65228 N 16929 1571 X66370 G ribosomal protein S9 ribosomal protein S9 20085 1572 X66870 C lamin A lamin A 495 1573 X68041 J superoxide dismutase 3 superoxide dismutase 3 417 1574 X70141 N 405 1575 X70223 M,H,K peroxisomal membrane protein 2 peroxisomal membrane protein 2 Table 1 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Title 24640 1576 X70521 N Sodium chanbnel, nonvoltage-gated 1, alpha (epithelial) Sodium channel, nonvoltage-gated 1, alpha (epithelial) complement component 1, q subcomponent, beta 21443 1577 X71127 M,L polypeptide complement component 1, q subcomponent, beta polypeptide 22219 1578 X72792 N,F alcohol dehydrogenase 1 alcohol dehydrogenase 1 1877 1579 X74593 A,D,E sorbitol dehydrogenase sorbitol dehydrogenase 15599 1580 X75253 J phosphatidylethanolamine binding protein phosphatidylethanolamine binding protein 24626 1581 X75856 N Testis enhanced gene transcript Testis enhanced gene transcript 16272 1582 X76456 N afamin afamin 1993 1583 X76985 M,E,G,K latexin latexin 24639 1584 X77932 N Sodium channel, nonvollage-gated, 1, beta (epithelial) Sodium channel, nonvoltage-gated 1, beta (epithelial) 23854 1585 X78327 N,G ribosomal protein L13 ribosomal protein L13 635 1586 X78848 N glutathiose S-transferase, alpha 1 glutahione S-transferase, alpha 1 13940 1587 X79321 N,D microbtubule-associated protein tau microtubule-associated protein tau 466 1588 X81395 N carboxylesterase 1 carboxylesterase 1 25747 1589 X81448 M,C,K keratin complex 1, acidic, gene 18 keratin complex 1, acidc, gene 18 570 1590 X82445 N nuclear distribution gene C homolog (Aspergillus)_ nuclear distribution gene C homolog (Aspergillus) 1764 1591 X83399 C eukaryotic translation initiation factor 4E eukaryolic translation initiation factor 4E 343 1592 X91810 L signal transducar and activator of transcription 3 signal transducer and activator of transcription 3 11849 1593 X93352 M,N,G ribosomal protein L10a ribosomal protein L10a 18107 1594 X94242 N ribosomal protein L14 ribosomal protein L14 12978 1595 X96437 M,H,I 25770 1595 x96437 N 21585 1596 X97772 D 3-phosphoglycerate dehydrogenase 3-phosphoglycarate dehydrogenase 21586 1596 X97772 D 3-phosphoglycerate dehydrogenase 3-phosphoglycerate dehydrogenase UDP-glucuronosyltransferase 283 precursor, 14347 1597 Y00156 N,H microsomal UDP-glucuronosyltransferase 283 precursor, microsomal 2629 1598 Y00396 K v-myc avian myelocytomalosis viral oncogene homolog v-myc avian myelocytomatosis viral oncogene homolog 4594 1599 Y07704 N Best5 protein Best5 protein 25777 1600 Y08355 M,A,F,I sequestosome 1 sequestosome 1 (cytosolic acyl-CoA thioesterase 1, mitochondrial acyl- 1858 1601 Y09333 B,L CoA thioesterase 1) (cytosolic acyl-CoA thioesterase 1, mitochondrial acyl-CoA thioesterase 1) Table 1 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Known Gene Name UniGene Cluster Title 15986 1602 Y09945 M,I putative integral membrane transport UST1r putative integral membrane transport UST1r 21914 1503 Y13336 J stress-induced-phosphoprotein 1 (Hsp70/Hsp90- 11840 1604 Y15068 H,I organizing protein) stress-induced-phosphoprotein 1 (Hsp70/Hsp90-organizing protein)_ 20173 1605 Z11932 N,C arginine vasopressin receptor 2 arginine vasopressin receptor 2 low density lipoprotein receptor-related protein 406 1606 Z11995 M associated protein 1 low density lipoprotein receptor-related protein associated protein 1 low density lipoprotein receptor-related protein 407 1606 Z11995 N,C associated protein 1 low density lipoprotein receptor-related protein associated protein 1 18352 1607 Z12298 L 23780 1608 Z19552 E topoisomerase (DNA) 2 alpha topoisomerase (DNA) 2 alpha 439 1609 Z22607 N,F Bone morphogenetic protein 4 Bone morphogenetic protein 4 494 1610 Z24721 J superoxide dismutase 3 superoxide dismutase 3 8663 1611 Z27118 N heat shock 70kD protein 1A heat shock 70kD protein 1A 17226 1612 Z36980 N,C,E D-dopachrome taulomerase D-dopachrome taulomerase 17227 1612 Z36980 N,E D-dopachrome taulomerase D-dopachrome taulomerase 6641 1613 Z49858 M,A,I plasmolipin plasmolipin 1542 1614 Z50144 N,J kynurenine aminotransferase 2 kynurenine aminotransferase 2 8664 1615 Z75029 N,C,D R.norvegicus hsp70.2 mRNA for heat shock protein 70 15569 1616 Z78279 N collagen, type 1, alpha 1 collagen, type 1, alpha 1 10887 1617 Z83757 M,I growth hormone receptor growth homone receptor Table 2 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Pathway Name activation of JNK Pathway via Pyk2 dependent signaling, BCR Signaling Pathway, Bioactive Peptide Induced Signaling Pathway, Ca++/Calmodulin-dependent Protein Kinase Activation, Control of skeletal myogenesis by HDAC & calcium/calmodulin-dependent kinase (CaMK), Corticosteroids and cardioprotection, Effects of calcineurin in Keratinocyte Differentiation, Fc Epsilon Receptor I Signaling in Mast Cells, Huntington's disease, Links between Pyk2 and Map Kinases, NFAT and Hypertrophy of the heart (Transcription in the broken heart), Neuropeptides VIP and PACAP inhibit the apoptosis of activated T cells, Nitric Oxide Signaling Pathway, Pertussis toxin-insensitive CCR5 Signaling in Macrophage, Phosphatidylinositol signaling system, Regulation of PGC-1a, Role of MEF2D in T-cell Apoptosis, Signaling Pathway from G-Protein Families, T Cell Receptor Signaling Pathway, fMLP induced 25802 1353 NM 031969 G, K chemokine gene expression in HMC-1 cells) (Activation of PKC through G protein coupled receptor, Aspirin Blocks Signaling Pathway Involved in Platelet Activation, CCR3 signaling in Eosinophils, Cadmium induces DNA synthesis and proliferation in macrophages, G-Protein Signaling Through Tubby Proteins, Inositol phosphate metabolism, PKC-catalyzed phosphorylation of inhibitory phosphoprotein of myosin phosphatase, Phosphatidylinositol signaling system, Phospholipase C Signaling Pathway, Phospholipids as signaling intermediaries, Regulation of ckl/cdk5 by type 1 glutamate receptors, Thrombin signaling and protease-activated receptors, fMLP induced chemokine gene 20414 1188 L14323 M expression in HMC-1 cells) (Acute Myocardial Infarction, Extrinsic Prothrombin Activation 556 1569 X64336 M, N Pathway, Intrinsic Prothrombin Activation Pathway) 46 1242 M23697 N (Acute Myocardial Infarction, Fibrinolysis Pathway) (Adhesion Molecules on Lymphocyte, Agrin in Postsynaptic Differentiation, Aspirin Blocks Signaling Pathway Involved in Platelet Activation, B Cell Survival Pathway, Cells and Molecules involved in local acute inflammatory response, Eph Kinases and ephrins support platelet aggregation, Erk and PI-3 Kinase Are Necessary for Collagen Binding in Corneal Epithelia, Erkl/Erk2 Mapk Signaling pathway, Integrin Signaling Pathway, Monocyte and its Surface Molecules, PTEN dependent cell cycle arrest and apoptosis, Ras- Independent pathway in NK cell-mediated cytotoxicity, Signaling of Hepatocyte Growth Factor Receptor, mCalpain and friends in Cell 14989 857 1177366 M, K motility, uCalpain and friends in Cell spread) (Adhesion Molecules on Lymphocyte, B Lymphocyte Cell Surface Molecules, CTL mediated immune response against target cells, Cells and Molecules involved in local acute inflammatory response, Monocyte and its Surface Molecules, Neutrophil and Its Surface Molecules, T Cytotoxic Cell Surface Molecules, T Helper Cell Surface 2554 1063 D00913 M, N Molecules) Table 2 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Pathway Name (Adhesion Molecules on Lymphocyte, B Lymphocyte Cell Surface Molecules, CTL mediated immune response against target cells, Cells and Molecules involved in local acute inflammatory response, Monocyte and its Surface Molecules, Neutrophil and Its Surface Molecules, T Cytotoxic Cell Surface Molecules, T Helper Cell Surface 2555 1063 D00913 M, C, I Molecules) (Agrin in Postsynaptic Differentiation, Angiotensin li mediated activation of JNK Pathway via Pyk2 dependent signaling, CBL mediated ligand-induced downregulation of EGF receptors, EGF Signaling Pathway, Erkl/Erk2 Mapk Signaling pathway, Keratinocyte Differentiation, Map Kinase Inactivation of SMRT Corepressor, Role of EGF Receptor Transactivation by GPCRs in Cardiac Hypertrophy, Sprouty regulation of tyrosine kinase signals, The role of FYVE-finger 17907 969 Api233224 M proteins in vesicle transport, mCalpain and friends in Cell motility) (AKAP95 roie in mnosis ana cnromosome dynamics, Acuvauon or Src by Protein-tyrosine phosphatase alpha, Cell Cycle: G1/S Check Point, Cell Cycle : G2/M Checkpoint, Cyclins and Cell Cycle Regulation, How Progesterone Initiates the Oocyte Maturation, Inositol phosphate metabolism, Nicotinate and nicotinamide metabolism, Protein Kinase A at the Centrosome, RB Tumor Suppressor/Checkpoint Signaling in response to DNA damage, Sonic Hedgehog (SHH) Receptor Ptc1 Regulates cell cycle, Sphingoglycolipid metabolism, Starch and sucrose metabolism, 21651 1560 X60767 N, E cdc25 and chk1 Regulatory Pathway in response to DNA damage) (AKAHuti roie in mitosis ana cnromosome dynamics, AKT Signaling Pathway, ChREBP regulation by carbohydrates and cAMP, Deregulation of CDK5 in Alzheimer Disease, Erkl/Erk2 Mapk Signaling pathway, Inactivation of Gsk3 by AKT causes accumulation of b-catenin in Alveolar Macrophages, Keratinocyte Differentiation, Protein Kinase A at the Centrosome, Regulation of ckl/cdk5 by type 1 glutamate receptors, Skeletal muscle hypertrophy is regulated via AKT/mTOR pathway, WNT Signaling Pathway, mTOR Signaling 3202 1527 X16043 N Pathway) (AKT Signaling Pathway, Actions of Nitric Oxide in the Heart, Ahr Signal Transduction Pathway, Corticosteroids and cardioprotection, Hypoxia and p53 in the Cardiovascular system, Hypoxia-Inducible Factor in the Cardiovascular System, Mechanism of Gene Regulation 16518 845 Al176546 N,C,K by Peroxisome Proliferators via PPAR(alpha)) (AKT Signaling Pathway, Actions of Nitric Oxide in the Heart, Ahr Signal Transduction Pathway, Corticosteroids and cardioprotection, Hypoxia and p53 in the Cardiovascular system, Hypoxia-Inducible Factor in the Cardiovascular System, Mechanism of Gene Regulation 20795 1360 NM 175761 N, H b Peroxisome Proliferators via PPARa (alpha)) Table 2 GLGC GenBank Ace or Model Identifier Seq ID RefSeq ID Code Pathway Name (AKT Signaling Pathway, Cell Cycle: G2/M Checkpoint, Control of skeletal myogenesis by HDAC & calcium/calmodulin-dependent kinase (CaMK), Multiple antiapoptotic pathways from IGF-1 R signaling lead to BAD phosphorylation, RB Tumor Suppressor/Checkpoint Signaling in response to DNA damage, Regulation of BAD phosphorylation, Regulation of PGC-1a, Regulation of cell cycle progression by Plk3, Role of nicotinic acetylcholine receptors in the regulation of apoptosis, Signal Dependent Regulation of Myogenesis by Corepressor MITR, cdc25 16683 1086 D17445 N and chkl Regulatory Pathwa in response to DNA damage) (AKT Signaling Pathway, Cell Cycle: G2/M Checkpoint, Control of skeletal myogenesis by HDAC & calcium/calmodulin-dependent kinase (CaMK), Multiple antiapoptotic pathways from IGF-1R signaling lead to BAD phosphorylation, RB Tumor Suppressor/Checkpoint Signaling in response to DNA damage, Regulation of BAD phosphorylation, Regulation of PGC-1 a, Regulation of cell cycle progression by Plk3, Role of nicotinic acetylcholine receptors in the regulation of apoptosis, Signal Dependent Regulation of Myogenesis by Corepressor MITR, cdc25 16684 1086 D17445 M and chk1 Regulatory Pathway in response to DNA damage) (AKT Signaling Pathway, Growth Hormone Signaling Pathway, Regulation of eIF4e and p70 S6 Kinase, The IGF-1 Receptor and 17524 559 Al010568 M, A, I Longevity) (AKT Signaling Pathway, Growth Hormone Signaling Pathway, Regulation of eIF4e and p70 S6 Kinase, The IGF-1 Receptor and 10887 1617 Z83757 M, l Longevity) (Alanine and aspartate metabolism, Arginine and proline metabolism, Cysteine metabolism, Glutamate metabolism, Phenylalanine metabolism, Phenylalanine, tyrosine and tryptophan biosynthesis, 17630 201 M892012 N Tyrosine metabolism) (Alanine and aspartate metabolism, Arginine and proline metabolism, 4234 457 AB016536 N K Urea cycle and metabolism of amino groups) (Alanine and aspartate metabolism, Arginine and proline metabolism, 18727 1078 D13978 N Urea cycle and metabolism of amino groups) (Alanine and aspartate metabolism, Arginine and proline metabolism, 20597 1512 X12459 N Urea cycle and metabolism of amino groups) (Alanine and aspartate metabolism, Butanoate metabolism, Glutamate metabolism, Taurine and hypotaurine metabolism, beta- 19824 1125 E13557 N, G, K Alanine metabolism) (Alanine and aspartate metabolism, Butanoate metabolism, Glutamate metabolism, Taurine and hypotaurine metabolism, beta- 19825 1288 M64755 N Alanine metabolism) (Alanine and aspartate metabolism, Citrate cycle (TCA cycle), Pyruvate metabolism, Shuttle for transfer of acetyl groups from 1478 1447 U32314 M mitochondria to the cytosol) (Alanine and aspartate metabolism, Citrate cycle (TCA cycle), Pyruvate metabolism, Shuttle for transfer of acetyl groups from 1479 1447 U32314 N, D mitochondria to the cytosol) (Alanine and aspartate metabolism, Glycerolipid metabolism, 15703 444 AB009372 N Phospholipid degradation) (Alanine and aspartate metabolism, Glycine, serine and threonine 7914 439 AB002584 N metabolism) 10789 947 Al232059 M (Alanine and aspartate metabolism, Histidine metabolism) Table 2 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Pathway Name (ALK in cardiac myocytes, Hop Pathway in Cardiac Development, NFAT and Hypertrophy of the heart (Transcription in the broken 15072 1357 NM_144730 A heart)) (Alzheimer's disease, Bioactive Peptide Induced Signaling Pathway, 13938 1339 NM 017212 N Deregulation of CDK5 in Alzheimer Disease, Parkinson's disease) (Alzheimer's disease, Bioactive Peptide Induced Signaling Pathway, 13939 1339 NM 017212 D Dere ulation of CDK5 in Alzheimer Disease, Parkinson's disease) (Alzheimer's disease, Bioactive Peptide Induced Signaling Pathway, 13940 1587 X79321 N, D Deregulation of CDK5 in Alzheimer Disease, Parkinson's disease) (Alzheimer's disease, Gamma-aminobutyric Acid Receptor Life 15376 153 M875206 N Cycle) 7488 464 AF007758 N (Alzheimer's disease, Parkinson's disease) 7489 464 AF007758 M, G, I, J, L |Alzheimer's disease, Parkinson's disease) (Aminosugars metabolism, Butanoate metabolism, Glycerolipid metabolism, Histidine metabolism, Lysine biosynthesis, Lysine degradation, Phenylalanine metabolism, Tyrosine metabolism, 20555 1439 U26033 F Valine, leucine and isoleucine degradation) (Amyotrophic lateral sclerosis (ALS), Apoptotic Signaling in Response to DNA Damage, Ceramide Signaling Pathway, Hypoxia and p53 in the Cardiovascular system, Regulation of BAD phosphorylation, Role of Mitochondria in Apoptotic Signaling, p53 912 1468 U59184 N Signaling Pathway) (Amyotrophic lateral sclerosis (ALS), Cardiac Protection Against ROS, Free Radical Induced Apoptosis, The IGF-1 Receptor and 20876 1238 M21060 J Longevity) 1853 1511 X12367 N (Amyotrophic lateral sclerosis (ALS), Glutathione metabolism) (Amyotrophic lateral sclerosis (ALS), Methane metabolism, The IGF- 15741 1214 M11670 N 1 Receptor and Lon evit, Tryptophan metabolism) (Androgen and estrogen metabolism, C21-Steroid hormone 275 1434 U22424 M metabolism) (Androgen and estrogen metabolism, C21-Steroid hormone 23660 747 Al105448 N metabolism, Visceral Fat Deposits and the Metabolic Syndrome) (Androgen and estrogen metabolism, Histidine metabolism, Selenoamino acid metabolism, Tryptophan metabolism, Tyrosine 20772 1470 U60882 N metabolism, Ubiquinone biosynthesis) (Androgen and estrogen metabolism, Mechanism of Gene 25070 1397 S83279 M, N Regulation by Peroxisome Proliferators via PPARa (alpha)) (Androgen and estrogen metabolism, Pentose and glucuronate interconversions, Porphyrin and chlorophyll metabolism, Starch and 5492 1097 D38061 N sucrose metabolism) (Androgen and estrogen metabolism, Pentose and glucuronate interconversions, Porphyrin and chlorophyll metabolism, Starch and 18028 1098 D38062 N sucrose metabolism) (Androgen and estrogen metabolism, Pentose and glucuronate interconversions, Porphyrin and chlorophyll metabolism, Starch and 1354 1099 D38065 N sucrose metabolism) (Androgen and estrogen metabolism, Pentose and glucuronate interconversions, Porphyrin and chlorophyll metabolism, Starch and 15126 1113 D83796 N sucrose metabolism) Table 2 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Pathway Name (Androgen and estrogen metabolism, Pentose and glucuronate interconversions, Porphyrin and chlorophyll metabolism, Starch and 15124 1134 J02612 N, B sucrose metabolism) (Androgen and estrogen metabolism, Pentose and glucuronate interconversions, Porphyrin and chlorophyll metabolism, Starch and 15125 1162 J05132 N, B sucrose metabolism) (Androgen and estrogen metabolism, Pentose and glucuronate interconversions, Porphyrin and chlorophyll metabolism, Starch and 14346 1252 M31109 N, B, H sucrose metabolism) (Androgen and estrogen metabolism, Pentose and glucuronate interconversions, Porphyrin and chlorophyll metabolism, Starch and 11755 1259 M33746 N, B, H sucrose metabolism) (Androgen and estrogen metabolism, Pentose and glucuronate interconversions, Porphyrin and chlorophyll metabolism, Starch and 5493 1369 S56936 N sucrose metabolism) (Androgen and estrogen metabolism, Pentose and glucuronate interconversions, Porphyrin and chlorophyll metabolism, Starch and 15127 1370 S56937 N sucrose metabolism) (Androgen and estrogen metabolism, Pentose and glucuronate interconversions, Porphyrin and chlorophyll metabolism, Starch and 17806 1407 U06273 N sucrose metabolism (Androgen and estrogen metabolism, Pentose and glucuronate interconversions, Porphyrin and chlorophyll metabolism, Starch and 17805 1408 U06274 N, B sucrose metabolism) (Androgen and estrogen metabolism, Pentose and glucuronate interconversions, Porphyrin and chlorophyll metabolism, Starch and 1537 1441 U27518 N, H sucrose metabolism) (Androgen and estrogen metabolism, Pentose and glucuronate interconversions, Porphyrin and chlorophyll metabolism, Starch and 14633 1499 X03478 H sucrose metabolism (Androgen and estrogen metabolism, Pentose and glucuronate interconversions, Porphyrin and chlorophyll metabolism, Starch and 14347 1597 Y00156 N,H sucrose metabolism) ########## ## ###### ########## ## #### ##### ### ### dependent signaling, BCR Signaling Pathway, CD40L Signaling Pathway, Ceramide Signaling Pathway, EGF Signaling Pathway, FAS signaling pathway (CD95), Fc Epsilon Receptor I Signaling in Mast Cells, HIV-I Nef: negative effector of Fas and TNF, Human Cytomegalovirus and Map Kinase Pathways, Inhibition of Cellular Proliferation by Gleevec, Inositol phosphate metabolism, Keratinocyte Differentiation, Links between Pyk2 and Map Kinases, MAPKinase Signaling Pathway, Map Kinase Inactivation of SMRT Corepressor, NF-kB Signaling Pathway, Neuropeptides VIP and PACAP inhibit the apoptosis of activated T cells, Nicotinate and nicotinamide metabolism, PDGF Signaling Pathway, Rac 1 cell motility signaling pathway, Role of MAL in Rho-Mediated Activation of SRF, Signal transduction through IL1R, Sphingoglycolipid metabolism, Starch and sucrose metabolism, T Cell Receptor Signaling Pathway, TNF/Stress Related Signaling, TNFR1 Signaling 1453 1456 U48596 F, K Pathway, TNFR2 Signaling Pathway, The 4-1 BB-dependent immune Table 2 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Pathway Name (########### ## ####### ######### ## #### ##### ### dependent signaling, BCR Signaling Pathway, CD40L Signaling Pathway, Ceramide Signaling Pathway, EGF Signaling Pathway, FAS signaling pathway (CD95), Fc Epsilon Receptor I Signaling in Mast Cells, HIV-I Nef: negative effector of Fas and TNF, Human Cytomegalovirus and Map Kinase Pathways, Inhibition of Cellular Proliferation by Gleevec, Inositol phosphate metabolism, Keratinocyte Differentiation, Links between Pyk2 and Map Kinases, MAPKinase Signaling Pathway, Map Kinase Inactivation of SMRT Corepressor, NF-kB Signaling Pathway, Neuropeptides VIP and PACAP inhibit the apoptosis of activated T cells, Nicotinate and nicotinamide metabolism, PDGF Signaling Pathway, Rac 1 cell motility signaling pathway, Role of MAL in Rho-Mediated Activation of SRF, Signal transduction through IL1R, Sphingoglycolipid metabolism, Starch and sucrose metabolism, T Cell Receptor Signaling Pathway, TNF/Stress Related Signaling, TNFR1 Signaling 1454 1456 U48596 M, K Pathway, TNFR2 Signaling Pathway, The 4-1 BB-dependent immune (Apoptotic DNA fragmentation and tissue homeostasis, Granzyme A 15434 531 A1008836 N mediated Apoptosis Pathway) (Apoptotic DNA fragmentation and tissue homeostasis, Granzyme A 15437 1114 D84418 E mediated Apoptosis Pathway) (Apoptotic Signaling in Response to DNA Damage, Caspase Cascade in Apoptosis, FAS signaling pathway (CD95), HIV-I Nef: negative effector of Fas and TNF, Huntington's disease, Induction of apoptosis through DR3 and DR4/5 Death Receptors, Role of 16116 475 AF025670 F Mitochondria in Apoptotic Signaling) (Apoptotic Signaling in Response to DNA Damage, Double Stranded RNA Induced Gene Expression, Eukaryotic protein translation, Regulation of elF2, Skeletal muscle hypertrophy is regulated via 4592 1135 J02646 H AKT/mTOR pathway) (Arginine and proline metabolism, Bile acid biosynthesis, Butanoate metabolism, Fatty acid metabolism, Glycerolipid metabolism, Glycolysis/Gluconeogenesis, Histidine metabolism, Lysine degradation, Phenylalanine metabolism, Propanoate metabolism, Pyruvate metabolism, Tryptophan metabolism, Tyrosine metabolism, 23884 1293 M73714 J Valine, leucine and isoleucine degradation, beta-Alanine metabolism) (Arginine and proline metabolism, Bile acid biosynthesis, Butanoate metabolism, Fatty acid metabolism, Glycerolipid metabolism, Glycolysis/Gluconeogenesis, Histidine metabolism, Lysine degradation, Propanoate metabolism, Pyruvate metabolism, Tryptophan metabolism, Valine, leucine and isoleucine degradation, 16884 723 103758 E beta-Alanine metabolism) (Arginine and proline metabolism, Bile acid biosynthesis, Butanoate metabolism, Fatty acid metabolism, Glycerolipid metabolism, Glycolysis/Gluconeogenesis, Histidine metabolism, Lysine degradation, Propanoate metabolism, Pyruvate metabolism, Tryptophan metabolism, Valine, leucine and isoleucine degradation, 16885 739 Al105188 K beta-Alanine metabolism) (Arginine and proline metabolism, Glutamate metabolism, Urea cycle 4574 968 Al233216 N and metabolism of amino groups) (Arginine and proline metabolism, Glycine, serine and threonine 16948 1151 J03588 N, A, C metabolism, Urea cycle and metabolism of amino groups) Table 2 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Pathwa Name (Arginine and proline metabolism, Glycine, serine and threonine 16775 1411 U07971 M, D, I, L metabolism, Urea cycle and metabolism of amino groups) (Arginine and proline metabolism, Glycine, serine and threonine 16947 1510 X08056 N metabolism, Urea cycle and metabolism of amino groups) (Arginine and proline metabolism, Urea cycle and metabolism of 4242 276 AA893325 N amino groups) (Arginine and proline metabolism, Urea cycle and metabolism of 4467 1274 M57664 N amino groups) (Arginine and proline metabolism, Urea cycle and metabolism of 25467 1321 M93297 N, G amino groups) (Arginine and proline metabolism, Urea cycle and metabolism of 1419 1492 U90887 N amino groups) (Arginine and proline metabolism, Urea cycle and metabolism of 23523 1509 X07944 N amino groups) (ATM Signaling Pathway, Amyotrophic lateral scierosis (ALS), Apoptotic Signaling in Response to DNA Damage, Cell Cycle : G1/S Check Point, Cell Cycle : G2/M Checkpoint, Chaperones modulate interferon Signaling Pathway, Double Stranded RNA Induced Gene Expression, Huntington's disease, Hypoxia and p53 in the Cardiovascular system, Overview of telomerase protein component gene hTert Transcriptional Regulation, RB Tumor Suppressor/Checkpoint Signaling in response to DNA damage, Regulation of cell cycle progression by Plk3, Regulation of transcriptional activity by PML, Tumor Suppressor Arf Inhibits 17377 1514 X13058 N Ribosomal Biogenesis, p53 Signaling Pathway) (ATM Signaling Pathway, Ceii Cyde : G1/S Check Point. Ceii Cyde : G2/M Checkpoint, Cyclins and Cell Cycle Regulation, Effects of calcineurin in Keratinocyte Differentiation, Erythropoietin mediated neuroprotection through NF-kB, Hypoxia and p53 in the Cardiovascular system, Influence of Ras and Rho proteins on G1 to 133 1436 U24174 N S Transition, p53 Signaling Pathway) (ATM Signaling Pathway, Cell Cycle : G2/M Checkpoint, Hypoxia and 352 661 AI070295 H p53 in the Cardiovascular system, p53 Signaling Pathway) (ATM Signaling Pathway, Cell Cycle : G2/M Checkpoint, Hypoxia and 353 1203 L32591 M,H,I p53 in the Cardiovascular system, p53 Signaling Pathway) (ATM Signaling Pathway, Cell Cycle : G2/M Checkpoint, Hypoxia and 354 1203 L32591 M, H, I p53 in the Cardiovascular system, p53 Signaling Pathway) 20841 1279 M58758 H (ATP synthesis, Oxidative phosphorylation 18449 1399 U00926 H (ATP synthesis, Oxidative phosphorylation) 20725 1541 X54510 A (ATP synthesis, Oxidative phosphorylation, Purine metabolism) (Bile acid biosynthesis, Fatty acid biosynthesis (path 2), Fatty acid 23698 1139 J02749 N, D metabolism, Valine, leucine and isoleucine degradation) (Bile acid biosynthesis, Fatty acid biosynthesis (path 2), Fatty acid 23699 1139 J02749 N, D, E metabolism, Valine, leucine and isoleucine degradation) (Bile acid biosynthesis, Fatty acid metabolism, Glycerolipid 22219 1578 X72792 N, F metabolism, Glycolysis/Gluconeogenesis, Tyrosine metabolism) 10260 1393 S81497 N (Bile acid biosynthesis, Glycerolipid metabolism) 25563 1393 S81497 N ile acid biosynthesis, Glycerolipid metabolismj (Blood group giycoiipid biosynthesis-lact series, Flood group glycolipid biosynthesis-neolact series, Fructose and mannose metabolism, Globoside metabolism, Glycerolipid metabolism, Keratan sulfate biosynthesis, N-Glycans biosynthesis, O-Glycans 10241 489 AF048687 N, C, K biosynthesis, Sphingoglycolipid metabolism) Table 2 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Pathway Name (Blood group glycolipid biosynthesis-neolact series, Keratan sulfate 4198 1305 M83143 M, N, I biosynthesis, N-Glycans biosynthesis) (Blood group glycolipid biosynthesis-neolact series, Keratan sulfate 4199 1305 M83143 M, N biosynthesis, N-Glycans biosynthesis) (Butanoate metabolism, Fatty acid biosynthesis (path 2), Fatty acid metabolism, Low-density lipoprotein (LDL) pathway during atherogenesis, Lysine degradation, Propanoate metabolism, Pyruvate metabolism, Synthesis and degradation of ketone bodies, 18956 1059 D00512 N Tryptophan metabolism) (Butanoate metabolism, Fatty acid biosynthesis (path 2), Fatty acid metabolism, Low-density lipoprotein (LDL) pathway during atherogenesis, Lysine degradation, Propanoate metabolism, Pyruvate metabolism, Synthesis and degradation of ketone bodies, 18958 1077 D13921 N Tryptophan metabolism) (Butanoate metabolism, Fatty acid biosynthesis (path 2), Fatty acid metabolism, Lysine degradation, Mechanism of Gene Regulation by Peroxisome Proliferators via PPARa (alpha), Propanoate metabolism, Tryptophan metabolism, Valine, leucine and isoleucine degradation, 17758 1173 K03249 N beta-Alanine metabolism) (Butanoate metabolism, Fatty acid biosynthesis (path 2), Fatty acid metabolism, Lysine degradation, Propanoate metabolism, Tryptophan metabolism, Valine, leucine and isoleucine degradation, 16768 1083 D16478 N beta-Alanine metabolism) (Butanoate metabolism, Fatty acid biosynthesis (path 2), Fatty acid metabolism, Lysine degradation, Propanoate metabolism, Tryptophan metabolism, Valine, leucine and isoleucine degradation, 21562 1525 X15958 N, A beta-Alanine metabolism) (Butanoate metabolism, Fatty acid biosynthesis (path 2), Fatty acid metabolism, Lysine degradation, Tryptophan metabolism, Valine, 15175 355 AA945583 E leucine and isoleucine degradation) (Butanoate metabolism, Methane metabolism, Pentose and 19252 204 AA892041 H glucuronate interconversions, Phenylalanine metabolism) (Butanoate metabolism, Methane metabolism, Pentose and 19254 467 AF014009 H glucuronate interconversions, Phenylalanine metabolism) 783 1011 AI236589 F(Butanoate metabolism, Pentose and glucuronate interconversions) (Butanoate metabolism, Synthesis and degradation of ketone bodies, 2812 809 Al171090 J Valine, leucine and isoleucine degradation) (Butanoate metabolism, Synthesis and degradation of ketone bodies, 15580 1258 M33648 N Valine, leucine and isoleucine degradation) (Cadmium induces DNA synthesis and proliferation in macrophages, Erkl/Erk2 Mapk Signaling pathway, IL-2 Receptor Beta Chain in T cell Activation, Inhibition of Cellular Proliferation by Gleevec, MAPKinase Signaling Pathway, Mechanism of Gene Regulation by Peroxisome Proliferators via PPARa (alpha), Neuropeptides VIP and PACAP inhibit the apoptosis of activated T cells, Overview of telomerase protein component gene hTert Transcriptional Regulation, Role of EGF Receptor Transactivation by GPCRs in Cardiac Hypertrophy, Tumor Suppressor Arf Inhibits Ribosomal 2629 1598 Y00396 K Biogenesis, WNT Signaling Pathway, p38 MAPK Signaling Pathway) Table 2 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Pathway Name ARM1 and Regulation of the Estrogen Receptor, Cell Cycle : G1/S Check Point, Cyclins and Cell Cycle Regulation, Inactivation of Gsk3 by AKT causes accumulation of b-catenin in Alveolar Macrophages, Influence of Ras and Rho proteins on G1 to S Transition, WNT 11434 1079 D14014 N, B Signaling Pathway, p53 Signaling Pathway) (CARM1 and Regulation of the Estrogen Receptor, Cell Cyde : G1/S Check Point, Cyclins and Cell Cycle Regulation, Inactivation of Gsk3 by AKT causes accumulation of b-catenin in Alveolar Macrophages, Influence of Ras and Rho proteins on G1 to S Transition, WNT 24232 1359 NM 171992 B Signaling Pathwa, p53 Signaling Pathway) (Caspase Cascade in Apoptosis, FAS signaling pathway (CD95), HIV-I Nef : negative effector of Fas and TNF, Induction of apoptosis through DR3 and DR4/5 Death Receptors, TNFR1 Signaling 20086 590 A1013260 M, H Pathway) (Caspase Cascade in Apoptosis, FAS signaling pathway (CD95), HIV-I Nef: negative effector of Fas and TNF, Induction of apoptosis through DR3 and DR4/5 Death Receptors, TNFR1 Signaling 20085 1572 X66870 C Pathway) (Caspase Cascade in Apoptosis, FAS signaling pathway (CD95), HIV-I Nef: negative effector of Fas and TNF, TNFR1 Signaling 3584 716 Al103106 E Pathway) (CBL mediated ! igand-induced downreguiation of EGF receptors, EGF Signaling Pathway, Keratinocyte Differentiation, Map Kinase Inactivation of SMRT Corepressor, Role of EGF Receptor Transactivation by GPCRs in Cardiac Hypertrophy, Sprouty regulation of tyrosine kinase signals, The role of FYVE-finger 20885 1403 U04842 N, G, K proteins in vesicle transport, mCalpain and friends in Cell motility) (CBL mediated ligand-induced downregulation of EGF receptors, EGF Signaling Pathway, Keratinocyte Differentiation, Map Kinase Inactivation of SMRT Corepressor, Role of EGF Receptor Transactivation by GPCRs in Cardiac Hypertrophy, Sprouty regulation of tyrosine kinase signals, The role of FYVE-finger 20884 1513 X12748 N, G, K proteins in vesicle transport, mCalpain and friends in Cell motility) (CCR3 signaling in Eosinophils, Rac 1 cell motility signaling pathway, 15364 742 AI105348 J Rho cell motility signaling pathway) (Cell to Cell Adhesion Signaling, Integrin Signaling Pathway, 21165 78 AA848941 K uCalpain and friends in Cell spread) (Cell to Cell Adhesion Signaling, Integrin Signaling Pathway, 21166 78 AA848941 K uCalpain and friends in Cell spread) (Citrate cycle (TCA cycle), Electron Transport Reaction in 17514 324 AA925554 E, G Mitochondria, Oxidative phosphorylation, Propanoate metabolism) (Citrate cycle (TCA cycle), Malate-aspartate shuttle, Pyruvate metabolism, Shuttle for transfer of acetyl groups from mitochondria to 4723 515 AF093773 N the cytoso) 165 778 AI145329 F (Citrate cycle (TCA cycle), Pyruvate metabolism) (Classical Complement Pathway, Complement Pathway, Lectin 15851 1453 U42719 M Induced Complement Pathway) (Controi of skeletal myogenesis by HDUC & calcium/calmodunn- dependent kinase (CaMK), Erythrocyte Differentiation Pathway, IGF- 1 Signaling Pathway, NFAT and Hypertrophy of the heart (Transcription in the broken heart), Regulation of BAD phosphorylation, Skeletal muscle hypertrophy is regulated via 21053 1226 M15481 M AKT/mTOR pathway, The IGF-1 Receptor and Longevity) Table 2 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Pathway Name (CXCR4 Signaling Pathway, Pertussis toxin-insensitive CCR5 4330 60 AA818747 M,B Signaling in Macrophage) (CXCR4 Signaling Pathway, Pertussis toxin-insensitive CCR5 24321 956 AI232340 M, K, L Signaling in Macrophage) 24778 1515 X13119 N Cysteine metabolism, Glycine, serine and threonine metabolism) (Cysteine metabolism, Glycolysis/Gluconeogenesis, Hypoxia- Inducible Factor in the Cardiovascular System, Propanoate 17807 1270 M54926 M, G metabolism, Pyruvate metabolism) (Cysteine metabolism, Glycolysis/Gluconeogenesis, Propanoate 7124 1409 U07181 E metabolism, Pyruvate metabolism, SARS Coronavirus Protease) (Cysteine metabolism, Methionine metabolism, Selenoamino acid 18452 1085 D17370 M, N metabolism (Cysteine metabolism, Methionine metabolism, Selenoamino acid 18453 1085 D17370 N, G metabolism) 15028 336 AA942685 N, F (Cysteine metabolism, Taurine and hypotaurine metabolism) 25024 1124 E03229 N (Cysteine metabolism, Taurine and hypotaurine metabolism) (Dendritic cells in regulating TH1 and TH2 Development, Glutathione metabolism, SARS Coronavirus Protease, Urea cycle and 1540 1246 M25073 N metabolism of amino groups) (Downregulated of MTA-3 in ER-negative Breast Tumors, Fructose and mannose metabolism, Glycolysis/Gluconeogenesis, Pentose 7064 1220 M12919 N phosphate pathway) (EGF Signaling Pathway, Erk1/Erk2 Mapk Signaling pathway, IL 6 signaling pathway, IL22 Soluble Receptor Signaling Pathway, PDGF Signaling Pathway, Signaling of Hepatocyte Growth Factor Receptor, 343 1592 X91810 L Stat3 Signaling Pathway, TPO Signaling Pathway) (Erk and PI-3 Kinase Are Necessary for Collagen Binding in Corneal 2109 47 AA817887 N, G Epithelia, Rho cell motility signaling pathway) 18713 585 Al012604 N, L (Eukaryotic protein translation, Regulation of eIF2) 18716 1345 NM020075 F (Eukaryotic protein translation, Regulation of elF2) (FAS signaling pathway (CD95), HIV-I Nef: negative effector of Fas and TNF, Induction of apoptosis through DR3 and DR4/5 Death Receptors, TNFR1 Signaling Pathway, uCalpain and friends in Cell 20741 510 AF084186 A, J spread) (FAS signaling pathway (CD95), HIV-I Nef : negative effector of Fas and TNF, Keratinocyte Differentiation, MAPKinase Signaling Pathway, Purine metabolism, Regulation of transcriptional activity by PML, Stress Induction of HSP Regulation, p38 MAPK Signaling 20849 1502 X05566 M, G, K Pathway) (Fatty acid metabolism, Glycerolipid metabolism, Mitochondrial 1977 1164 J05470 N, L Carnitine Palmitoyltransferase (CPT) System) (Fatty acid metabolism, Glycerolipid metabolism, Mitochondrial Carnitine Palmitoyltransferase (CPT) System, Reversal of Insulin 15411 1178 L07736 N, B, L Resistance by Leptin) (Fatty acid metabolism, Glycolysis/Gluconeogenesis, Propanoate 13004 1007 AI236284 J, L metabolism, Pyruvate metabolism) (Fatty acid metabolism, Glycolysis/Gluconeogenesis, Propanoate 13005 1116 D85189 N, C metabolism, Pyruvate metabolism) (Fatty acid metabolism, Mechanism of Acetaminophen Activity and 4011 496 AF056333 N, J Toxicity, Tryptophan metabolism) (Fatty acid metabolism, Mechanism of Acetaminophen Activity and 4012 1367 S48325 N, J Toxicity, Tryptophan metabolism) Table 2 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Pathway Name (Fatty acid metabolism, Mechanism of Gene Regulation by 16150 11 AA799489 G Peroxisome Proliferators via PPARa (alpha)) (Fatty acid metabolism, Mechanism of Gene Regulation by 16148 1140 J02752 N Peroxisome Proliferators via PPARa (alpha)) (Fatty acid metabolism, Propanoate metabolism, Valine, leucine and 21078 1143 J02791 N, G isoleucine degradation, beta-Alanine metabolism) (Fatty acid metabolism, Prostaglandin and leukotriene metabolism, 20716 1323 M94548 G Tryptophan metabolism) 1174 1136 J02657 N Fatt acid metabolism, Tryptophan metabolism) 67 1268 M37828 B (Fatty acid metabolism, Tryptophan metabolism) 14997 1150 J03572 N (Folate biosynthesis, Glycerolipid metabolism) 14996 1526 X16038 M, D (Folate biosynthesis, Glycerolipid metabolism) (Folate biosynthesis, Histidine metabolism, Phenylalanine 1431 632 A1044610 D metabolism, Tryptophan metabolism, Tyrosine metabolism) (Folate biosynthesis, Histidine metabolism, Phenylalanine 1430 1309 M84648 M metabolism, Tryptophan metabolism, Tyrosine metabolism) 1549 1166 J05519 G (Folate biosynthesis, One carbon pool by folate) (Free Radical Induced Apoptosis, Glutamate metabolism, 6405 1208 L38615 G Glutathione metabolism) (Free Radical Induced Apoptosis, Glutamate metabolism, 6406 1208 L38615 N Glutathione metabolism) 21975 827 Al172247 N, B, L (Free Radical Induced Apoptosis, Purine metabolism) (Fructose and mannose metabolism, Galactose metabolism, 1340 1437 U25651 B Glycolysis/Gluconeogenesis, Pentose phosphate pathway) (Fructose and mannose metabolism, Glycolysis/Gluconeogenesis, 820 225 AA892395 N Glycolysis Pathway, Pentose phosphate pathway) (Fructose and mannose metabolism, Glycolysis/Gluconeogenesis, 818 1497 X02291 N Glycolysis Pathway, Pentose phosphate pathway) (Fructose and mannose metabolism, Glycolysis/Gluconeogenesis, 16895 1313 M86240 N Pentose phosphate pathway) (FXR and LXR Regulation of Cholesterol Metabolism, Mechanism of 968 1119 D86745 G, K Gene Regulation by Peroxisome Proliferators via PPARa (alpha)) (Galactose metabolism, Glycolysis/Gluconeogenesis, Starch and 1321 1206 L37333 N sucrose metabolism) 1622 1300 M80804 N (Galactose metabolism, Starch and sucrose metabolism) 1247 1163 J05181 N, J (Glutamate metabolism, Glutathione metabolism) 14003 1374 S65555 N, B, J (Glutamate metabolism, Glutathione metabolism) 20817 582 A1012589 M, N (Glutathione metabolism, Multi-Drug Resistance Factors) 20818 1498 X02904 M, N (Glutathione metabolism, Multi-Drug Resistance Factors) 1399 1508 X07467 M, H, I (Glutathione metabolism, Pentose phosphate pathway) (Glutathione metabolism, Prostaglandin and leukotriene metabolism, 35 1260 M33822 C Selenoamino acid metabolism, Taurine and hypotaurine metabolism) (Glutathione metabolism, Prostaglandin and leukotriene metabolism, 33 1500 X03518 N Selenoamino acid metabolism, Taurine and hypotaurine metabolism) (Glycerolipid metabolism, Glycolysis/Gluconeogenesis, Pentose 23109 1072 D10854 N and glucuronate interconversions) 755 1100 D38448 M, N (Glycerolipid metabolism, Phosphatidylinositol signaling system) 754 1336 NM_013126 N (Glycerolipid metabolism, Phosphatidylinositol signaling system) (Glycerolipid metabolism, Phospholipid degradation, Prostaglandin 25279 1092 D30740 C and leukotriene metabolism) Table 2 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Pathway Name (Glycerolipid metabolism, Phospholipid degradation, Prostaglandin 16147 1459 U51898 M, N and leukotriene metabolism) (Glycerolipid metabolism, Phospholipid degradation, Rac 1 cell 1535 437 AB000778 F motility signaling pathway, Ras Signaling Pathway) (Glycine, serine and threonine metabolism, Hemoglobin"s 16448 1117 D86297 N Chaperone) (Glycine, serine and threonine metabolism, Huntington's disease, 291 1316 M88347 M, N, F Methionine metabolism, Selenoamino acid metabolism) 1312 1255 M31788 (Glycolysis/Gluconeogenesis, Glycolysis Pathway) (Glycolysis/Gluconeogenesis, Glycolysis Pathway, Purine 20513 1503 X05684 N metabolism, Pyruvate metabolism) (Glycolysis/Gluconeogenesis, Histidine metabolism, Phenylalanine 15876 241 AA892582 N, G metabolism, Tyrosine metabolism) 18564 33 AA800745 M Hemoglobin"s Chaperone, Por h rin and chlorophyll metabolism) (HIV-I Nef : negative effector of Fas and TNF, Phosphatidylinositol 25405 1230 M18330 N signaling system) 20809 1229 M17069 N, D (Huntington's disease, Phosphatidylinositol signaling system) 20518 1520 X14265 N Huntington's disease, Phosphatidylinositol signaling system) (Hypoxia and p53 in the Cardiovascular system, Multi-Drug 5733 1303 M81855 N Resistance Factors) 1698 1137 J02679 M, B H (Hypoxia and p53 in the Cardiovascular system, Sterol biosynthesis) (IL-10 Anti-inflammatory Signaling Pathway, Porphyrin and 16081 888 AI179610 N chlorophyll metabolism) (IL-10 Anti-inflammatory Signaling Pathway, Porphyrin and 16080 1138 J02722 N chlorophyll metabolism) (Inositol metabolism, Propanoate metabolism, Valine, leucine and 10087 817 Al171803 M isoleucine degradation) (Inositol metabolism, Propanoate metabolism, Valine, leucine and 17269 1322 M93401 M isoleucine degradation) (Inositol phosphate metabolism, MAPKinase Signaling Pathway, Nicotinate and nicotinamide metabolism, Sphingoglycolipid 14956 1286 M64301 N metabolism, Starch and sucrose metabolism) (Inositol phosphate metabolism, MAPKinase Signaling Pathway, Nicotinate and nicotinamide metabolism, Sphingoglycolipid 14957 1286 M64301 N metabolism, Starch and sucrose metabolism) (Inositol phosphate metabolism, MAPKinase Signaling Pathway, Nicotinate and nicotinamide metabolism, Sphingoglycolipid 6577 1506 X06942 F metabolism, Starch and sucrose metabolism) (Inositol phosphate metabolism, Nicotinate and nicotinamide metabolism, Phosphatidylinositol signaling system, Sphingoglycolipid 21029 24 M799981 C metabolism, Starch and sucrose metabolism) 1542 1614 Z50144 N, J (Lysine biosynthesis, Lysine degradation, Tryptophan metabolism) (Malate-aspartate shuttle, Shuttle for transfer of acetyl groups from 23300 1488 U84727 N mitochondria to the cytosol) (Mechanism of Gene Regulation by Peroxisome Proliferators via 20896 1475 U64030 A, F PPARa (alpha), Pyrimidine metabolism) 1069 1522 X15096 N (Methane metabolism, Phenylalanine metabolism, Ribosome (NFAT and Hypertrophy of the heart (Transcription in the broken 15295 164 AA875594 M, H, I heart, mTOR Signaling Pathway) (NFAT and Hypertrophy of the heart (Transcription in the broken 6782 838 AI176170 B heart), mTOR Signaling Pathway) Table 2 GLGC GenBank Acc or Model Identifier Se ID RefSeq ID Code Pathway Name (NFAT and Hypertrophy of the heart (Transcription in the broken 15296 907 Al228738 N, H, I heart), mTOR Signaling Pathway) (NFAT and Hypertrophy of the heart (Transcription in the broken 15297 1118 D86641 N, K heart), mTOR Signaling Pathway) (Nucleotide sugars metabolism, Pentose and glucuronate 18597 455 AB013732 N, B, H interconversions, Starch and sucrose metabolism) 21211 433 AB000098 C (Oxidative phosphorylation, Ubiquinone biosynthesis) 20173 1605 Z11932 N, C (Oxidative phosphorylation, Ubiquinone biosynthesis) (Pantothenate and CoA biosynthesis, Pyrimidine metabolism, beta- 811 1110 D63704 M, l Alanine metabolism) (Pantothenate and CoA biosynthesis, Pyrimidine metabolism, beta- 812 1110 D63704 M, l Alanine metabolism) (Pantothenate and CoA biosynthesis, Pyrimidine metabolism, beta- 1508 1332 M97662 N, G Alanine metabolism) (Pantothenate and CoA biosynthesis, Valine, leucine and isoleucine 24643 1477 U68417 N, K biosynthesis, Valine, leucine and isoleucine degradation) 24582 1528 X16554 D Pentose phosphate pathway, Purine metabolism) 1847 1529 X16555 B (Pentose phosphate pathway, Purine metabolism) (Phenylalanine, tyrosine and tryptophan biosynthesis, Tryptophan 6055 1218 M12337 M, N, D metabolism) (Presenilin action in Notch and Wnt signaling, Proteolysis and Signaling Pathway of Notch, g-Secretase mediated ErbB4 Signaling 13485 1057 AJ012603 B Pathway) 24885 1088 D25224 N (Prion disease, Ribosome) 20481 1240 M22631 M, N, G, K (Propanoate metabolism, Valine, leucine and isoleucine degradation) (PTEN dependent cell cycle arrest and apoptosis, Regulation of eIF4e and p70 S6 Kinase, Skeletal muscle hypertrophy is regulated 1928 1418 U10357 N via AKT/mTOR pathway, mTOR Signaling Pathway) (PTEN dependent cell cycle arrest and apoptosis, Regulation of eIF4e and p70 S6 Kinase, Skeletal muscle hypertrophy is regulated 1929 1418 U 10357 N, A, C, D, E via AKT/mTOR pathway, mTOR Signaling Pathway) 23709 1356 Nom 138532 N (Purine metabolism, Pyrimidine metabolism) (Regulation of eIF4e and p70 S6 Kinase, Skeletal muscle hypertrophy is regulated via AKT/mTOR pathway, mTOR Signaling 1570 1404 U05014 A Pathway) (Regulation of Spermatogenesis by CREM, Repression of Pain 355 1375 S66024 N Sensation by the Transcriptional Regulator DREAM) (Regulation of Spermatogenesis by CREM, Repression of Pain 356 1375 S66024 N Sensation by the Transcriptional Regulator DREAM) (Ribosome, Skeletal muscle hypertrophy is regulated via AKT/mTOR 17104 1251 M29358 M, G pathway, mTOR Signaling Pathway) (Ribosome, Skeletal muscle hypertrophy is regulated via AKT/mTOR 17105 1251 M29358 N pathway, mTOR Signaling Pathway) (Sonic Hedgehog (SHH) Receptor Ptc1 Regulates cell cycle, Sonic 605 1199 L27340 C Hedgehog (Shh) Pathway) 16681 1095 D37920 N, B, L (Sterol biosynthesis, Terpenoid biosynthesis) 15069 1319 M89945 H (Sterol biosynthesis, Terpenoid biosynthesis) 25460 1319 M89945 N (Sterol biosynthesis, Terpenoid biosynthesis) 16449 1327 M95591 N (Sterol biosynthesis, Terpenoid biosynthesis) 16450 1327 M95591 N (Sterol biosynthesis, Terpenoid biosynthesis) 19058 493 AF054618 E Agrin in Postsynaptic Differentiation 18008 1350 NM_031588 N Agrin in Postsynaptic Differentiation Table 2 GLGC GenBank Acc or Model Identifier Seq ID RefSe ID Code Pathwa Name 18005 1401 U02320 N Agrin in Postsynaptic Differentiation 18011 1402 U02322 M, H Agrin in Postsynaptic Differentiation 347 1400 U01914 D AKAP95 role in mitosis and chromosome dynamics 439 1609 Z22607 N, F ALK in cardiac myocytes 1515 1064 D10233 J Aminosugars metabolism 9125 67 AA819338 N Am otrophic lateral sclerosis (ALS) 8426 483 AF036335 N, E, F Antisense Pathway 23778 298 AA899854 N, E Apoptotic DNA fragmentation and tissue homeostasis 19110 1289 M64986 A, J Apoptotic DNA fragmentation and tissue homeostasis 23780 1608 Z19552 E Apoptotic DNA fragmentation and tissue homeostasis 14638 765 137049 J ATM Signaling Pathway 16398 1478 U75392 N CARM1 and Regulation of the Estrogen Receptor 6758 592 A1013394 B, L Chondroitin/Heparan sulfate biosynthesis 15385 249AA892808 NCitrate cycle (TCA cycle) 19991 730 AI103956 K Citrate cycle (TCA cycle) 17516 847 AI176621 A,E, L Citrate cycle (TCA cycle) 7197 820 AI171962 M,G,K, L Corticosteroids and cardioprotection 7196 1371 S57478 M, E, G, K Corticosteroids and cardioprotection 16354 1108 D50564 N, C Cysteine metabolism 1081 466 AF013145 M, D Downregulated of MTA-3 in ER-negative Breast Tumors 19998 964 AI232999 M Downregulated of MTA-3 in ER-negative Breast Tumors 1462 999 Al235585 M, E, G Downregulated of MTA-3 in ER-negative Breast Tumors 1463 1540 X54467 M, G, K Downregulated of MTA-3 in ER-negative Breast Tumors 17563 875 AI178570 N Eukaryotic protein translation 24874 1410 U07619 N Extrinsic Prothrombin Activation Pathway 20711 307AA924267 N, L Fatty acid metabolism 15926 451 AB012933 Fatty acid metabolism 20983 634 A1044900 K Fatt acid metabolism 18687 804 Al170568 N Fatty acid metabolism 18686 1062 D00729 N Fatty acid metabolism 6780 1160 J05029 N Fatty acid metabolism 20713 1275 M57718 N, J, L Fatty acid metabolism 20715 1507 X07259 N, L Fatty acid metabolism 15540 1243 M24067 K Fibrinolysis Pathway 13479 1149 J03481 N Folate biosynthesis 13480 1149 J03481 N Folate biosynthesis 21400 1266 M36410 C, F Folate biosynthesis 1527 1299 M77850 B Folate biosynthesis M, N, E, G, H 16726 1352 NM 031855, I Fructose and mannose metabolism 1877 1579 X74593 A, D, E Fructose and mannose metabolism 1214 1076 D13871 M, N, K FXR and LXR Regulation of Cholesterol Metabolism 19712 1429 U18374 K FXR and LXR Regulation of Cholesterol Metabolism 5384 166 AA891041 I GATA3 participate in activating the Th2 cytokine genes expression 989 1464 U56242 N, D, F GATA3 participate in activating the Th2 cytokine genes expression 20161 1543 X54686 M, C, I GATA3 participate in activating the Th2 cytokine genes expression 5206 327 AA925755 E Glutamate metabolism 20717 844 AI176504 N Glutamate metabolism 11153 1320 M91652 N Glutamate metabolism 4615 1061 D00680 N Glutathione metabolism 21011 1128 H32189 N Glutathione metabolism 21012 1133 J02592 N, B Glutathione metabolism 21013 1144 J02810 N Glutathione metabolism Table 2 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Pathway Name 15017 1153 J03752 N, B Glutathione metabolism 21014 1155 J03914 B, L Glutathione metabolism 18989 1168 K00136 N Glutathione metabolism 634 1170 K01932 N Glutathione metabolism 25525 1383 S72505 N Glutathione metabolism 635 1586 X78848 N Glutathione metabolism 20753 43 M801441 M, N, C, I Glycerolipid metabolism 22554 353 AA945076 M,I Glycerolipid metabolism 3512 442 AB006607 F Glycerolipid metabolism 1306 1065 D10262 N Glycerolipid metabolism 17684 220 AA892345 M, I GI cine, serine and threonine metabolism 21587 293 AA899141 D Glycine, serine and threonine metabolism 21038 1148 J03190 H Glycine, serine and threonine metabolism 21039 1148 J03190 H Glycine, serine and threonine metabolism 1550 1504 X06150 N Glycine, serine and threonine metabolism 1551 1504 X06150 N, G Glycine, serine and threonine metabolism 21585 1596 X97772 D Glycine, serine and threonine metabolism 21586 1596 X97772 D Glycine, serine and threonine metabolism 187 1094 D32209 F Granzyme A mediated Apoptosis Pathway M, N, H, I, J, 20801 1104 D44495 L Granzyme A mediated Apoptosis Pathway 1685 97 AA851497 J Hemoglobin"s Chaperone 17832 573 Al012182 J Hemoglobin"s Chaperone 17833 868 Ai177992 F Hemogiobin"s Chaperone 17829 884 AI179576 N,J Hemoglobin"s Chaperone 1687 890 AI179971 J Hemoglobin"s Chaperone 1688 932 Al230970 Hemoglobin"s Chaperone 1689 1009 AI236360 J Hemoglobin"s Chaperone 25468 1324 M94918 N,J Hemoglobin"s Chaperone 1684 1547 X56325 J Hemoglobin"s Chaperone 3610 776 AI145151 M,G,I, J Histidine metabolism 3608 1067 D10693 M, J Histidine metabolism 3609 1395 S82579 N, F Histidine metabolism 17154 1228 M15883 Huntington's disease 15097 535 AI009405 N Hypoxia and p53 in the Cardiovascular system 1424 1423 U14746 N H poxia-Inducible Factor in the Cardiovascular System 4392 906 AI228674 H IL-2 Receptor Beta Chain in T cell Activation Inactivation of Gsk3 by AKT causes accumulation of b-catenin in 15393 806 AI170663 J Alveolar Macrophages 7888 976 AI233583 M inhibition of Matrix Metalloproteinases 17550 565 AI011607 M, l Lysine degradation 1814 1253 M31174 N Map Kinase Inactivation of SMRT Corepressor 15701 447 AB010467 A, I Multi-Drug Resistance Factors 21575 1544 X55298 J N-Glycans biosynthesis 12606 1281 M59861 N, E, K One carbon ool by folate 11953 703 Al102505 A Oxidative phosphorylation 11955 1212 L48209 N Oxidative phosphorylation 23225 1249 M27467 N Oxidative phosphorylation 11956 1250 M28255 N Oxidative phosphorylation 1598 1445 U30186 N p38 MAPK Signaling Pathway 11454 1245 M24604 M p53 Signaling Pathway 11455 1245 M24604 _ p53 Signaling Pathway 24821 1066 D10392 J Parkinson's disease Table 2 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Pathwa Name 16039 9 AA799452 H Pentose phosphate pathwa 20804 567 AI011684 H Pentose phosphate pathway 20802 655 AI059508 N, H Pentose phosphate pathway 20803 1413 U09256 N,B,H,I Pentose phosphate pathway 1183 465 AF013144 N Phosphatidylinositol signaling system 14978 858 AI177386 f Phosphatidylinositol signaling system 245 1107 D45412 J Phosphatidylinositol signaling system 1712 1177 L06096 M Phosphatidylinositol signaling system 24219 1200 L27843 M,L Phosphatidylinositol signaling system 1844 1261 M33962 J Phosphatidylinositol signaling system 1824 1427 U17971 K Phosphatidylinositol signaling system 247 1443 U28938 J'hosphatidylinositol signaling system 7700 744 AI105383 M,D Phospholipids as signalling intermediaries Phosphorylation of MEK1 by cdk5/p35 down regulates the MAP 23868 474 AF023087 M, L kinase pathway Phosphorylation of MEK1 by cdk5/p35 down regulates the MAP 23872 1231 M18416 M kinase pathway Phosphorylation of MEK1 by cdk5/p35 down regulates the MAP 23869 1479 U75397 L kinase pathway 16521 557 A1010470 B, J, L Porphyrin and chlorophyll metabolism 16520 1204 L33869 M, B, C, L Porphyrin and chlorophyll metabolism 17554 1115 D85100 N Propanoate metabolism 15538 758 AI112633 L Proteasome 25253 1068 D10754 H Proteasome 15535 1069 D10755 L Proteasome 3254 1070 D10756 N, L Proteasome 4003 1071 D10757 N Proteasome 1884 1109 D50695 I Proteasome 3987 1122 D90258 M, N Proteasome 15470 1466 U57050 H Proteasome 1447 1545 X55986 D Proteasome 8888 81 AA849036 N, B Purine metabolism 14184 126 M859837 M Purine metabolism 14185 126 M859837 M Purine metabolism 2979 289 AA894099 H Purine metabolism 4327 501 AF063447 M, G, I Purine metabolism 1466 1222 M14050 N Purine metabolism 1246 1273 M57507 M, J Purine metabolism 1970 1446 U31463 N, K Purine metabolism 16708 1465 U57042 M, N Purine metabolism 20483 1524 X15939 N Purine metabolism 24235 169 AA891286 M, N, H, I Pyrimidine metabolism 24234 1474 U63923 M, A, I Pyrimidine metabolism 1409 589 A1012802 M, A, C, E, F Pyruvate metabolism 240 1297 M75153 N Rab GTPases Mark Targets In The Endocytotic Machinery 1867 91 AA850940 N Ribosome 20839 177 AA891729 N Ribosome 4259 207 AA892123 N Ribosome 20812 356 AA945611 N Ribosome 19268 530 A1008641 D Ribosome 815 603 A1014087 N Ribosome 16918 715 AI103074 N Ribosome Table 2 GLGC GenBank Acc or Model Identifier Seq ID RefSeq ID Code Pathway Name 14929 802 AI170353 M,G, K Ribosome 18612 904 Al228624 Ribosome 15468 997 Al235364 N Ribosome 19112 1036 Al639157 J Ribosome 10878 1174 K03250 N Ribosome 24615 1318 M89646 N, D Ribosome 15135 1382 S71021 N, G Ribosome 16204 1505 X06423 M, N, G Ribosome 16205 1505 X06423 N, F Ribosome 16847 1516 X13549 N Ribosome 9620 1535 X53377 N Ribosome 10267 1550 X57432 N Ribosome 16929 1571 X66370 G Ribosome 23854 1585 X78327 N, G Ribosome 11849 1593 X93352 M, N, G Ribosome 18107 1594 X94242 N Ribosome 4361 1127 H31839 N Role of Mitochondria in Apoptotic Signaling 8829 1271 M55015 M, A, F, K SARS Coronavirus Protease 18354 1559 X59859 J Small Leucine-rich Proteoglycan (SLRP) molecules 24192 306 AA924210 H Sterol biosynthesis 15242 459 AB017912 D TGF beta signaling pathway 15243 459 AB017912 N TGF beta signaling pathway 17324 495 AF056031 Tryptophan metabolism 20493 1090 D28339 M, N Tryptophan metabolism 20494 1103 D44494 N, E Tryptophan metabolism 794 1476 U68168 M, I Tryptophan metabolism 23961 1298 M77694 M, N, E, G, I Tyrosine metabolism 15277 989 AI234889 D Ubiquitin mediated proteolysis 17378 1284 M62388 N, D Ubiquitin mediated proteolysis 15273 1421 U13177 E Ubiquitin mediated proteolysis 21950 599 A1013861 N, G Valine, leucine and isoleucine degradation 4449 712 Al102838 N, B, G, K Valine, leucine and isoleucine degradation 17284 1145 J02827 N, G Valine, leucine and isoleucine degradation 17285 1145 J02827 N Valine, leucine and isoleucine degradation 4450 1161 J05031 N, E Valine, leucine and isoleucine degradation 4451 1161 J05031 M, N, F Valine, leucine and isoleucine degradation 21072 28AA800211KVitamin B6 metabolism 16248 1376 S68135 N Vitamin C in the Brain Table 3 GLGC GenBank Acc or dentifier Seq ID RefSeq ID Model Code Human Homologous Gene Name Human Homologous Cluster Title (2,4-dienoyl CoA reductase 2, peroxisomal, 2-4-dienoyl- (2,4-dienoyl CoA reductase 2, peroxisomal, 2-4-diencyl-Coenzyme 22603 487 AF044574 N Coenzyme A reductase 2, peroxisomal) A reductase 2 peroxisomal) (3-hydroxy-3-methylglutaryl-Coenzyme A lyase, 3-hydroxymethyl- 3-methylglutaryl-Coenzyme A lyase (3-hydroxy-3-methylglutaryl-Coenzyme A lyase, 3-hydroxymethyl-3- 2812 809 AI171090 J (hydroxymethylglutaricaciduria)) methylglutaryl-Coenzyme A lyase (hydroxymethylglutaricaciduria)) (3-hydroxy-3-methylglutaryl-Coenzyme A reductase, HMG 24192 306 AA924210 H Coenzyme A reductase, Hydroxymethylglutaryl-coA reductase) 3-hydroxy-3-methylglutaryl-Coenzyme A reductase (3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2, 3-hydroxy- 3-methylglutaryl-Coenzyme A synthase 2 (mitochondrial), (3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2, 3-hydroxy-3- 15580 1258 M33648 N hydroxymethlglutaryl-CoA synthase) methylglutaryl-Coenzyme A synthase 2 (mitochondrial)) (3-hydroxyacyl-CoA dehydrogenase, hydroxyacyl-Coenzyme A hydroxyacyl-Coenzyme A dehydrogenase/3-ketoacyl-Coenzyme A dehydrogenase/3-ketoacyl-Coenzyme A thiolase/enoyl- thiolase/enoyl-Coenzyme A hydratase (trifunctional protein), alpha 16768 1083 D16478 N Coenzyme A hydratase (trifunctional protein), alpha subunit0 subunit (3-HYDROXYISOBUTYRATE DEHYDROGENASE PRECURSOR (EC 1.1.1.31) (HIBADH) (FRAGMENT), 3- hydroxyisobutyrate dehydrogenase, RIKEN cDNA 6430402H10 (3-hydroxyisobutyrate dehydrogenase, RIKEN cDNA 6430402H10 21950 599 AI013861 N,G gene) gene) (40S ribosomal protein S13, Ribosomal protein S13, ribosomal 20427 1536 X53378 N protein S13) ribosomal protein S13 (40S ribosomal protein S13, Ribosomal protein S13, ribosomal 20427 1536 X53378 N protein S13) ribosomal protein S13 (40S ribosomal protein S26, Ribosomal protein S26, ribosomal 815 603 AI014087 N protein S26, similar to 40S ribosomal protein S26) ribosomal protein S26 (40S ribosomal protein S6, Ribosomal protein S6, ribosomal 17104 1251 M29358 M,G protein S6) ribosomal protein S6 (40S ribosomal protein S6, Ribosomal protein S6, ribosomal 17104 1251 M29358 M,G protein S6) ribosomal protein 86 (40S ribosomal protein S6, Ribosomal protein S6, ribosomal 17105 1251 M29358 N protein S6) ribosomal protein S6 (40S ribosomal protein, laminin receptor 1 (ribosomal protein (laminin receptor 1 (ribosomal protein SA), laminin receptor 1 24885 1088 D25224 N SA), laminin receptor 1 (ribosomal protein SA, 67kDa)) (ribosomal protein SA, 67kDa)) 15468 997 AI235364 N (40S ribosomal protein, ribosomal protein S15a) ribosomal protein S15a (6-pyruvoyl-tetrahydropterin synthase, 6-pyruvoyltetrahydropterin (6-pyruvoyl-tetrahydropterin synthase, 6-pyruvoyltetrahydropterin 1527 1299 M77850 B synthase, purple) synthase) Table 3 GLGC GenBank Acc or identifier Seq ID RefSeq ID Model Code Human Homologous Gene Name Human Homologous Cluster Title (6-pyruvoyl-tetrahydropterin synthase/dimerization cofactor of hepatocyte nuclear factor 1 alpha (TCF1). pterin-4a- 6-pyruvoyl-tetrahydropterin synthase/dimerization cofactor of 21882 1308 M83740 M,N,D carbinolamine dehydratase) hepatocyte nuclear factor 1 alpha (TCF1) 9a disintegrin and metalloproteinase domain 17, a disintegrin and (a disintegrin and metalloproteinase domain 17, a disintegrin and metalloproteinase domain 17 (tumor necrosis factor, alpha, metalloproteinase domain 17 (tumor necrosis factor, alpha, 13485 1057 AJ012603 B converling enzyme)) converting enzyme)) (acetoacetyl CoA thiolase, acetyl-Coenzyme A acetyltransferase 1, acetyl-Coenzyme A acetyltransferase 1 (acetoacetyl (acetyl-Coenzyme A acetyltransferase 1, acetyl-coenzyme A 18956 1059 D00512 N Coenzyme A thiolase)) acetyltransferase 1 (acetoacetyl Coenzyme A thiolase)) (acetoacetyl CoA thiolase, acetyl-Coenzyme A acetyltransferase 1, acetyl-Coenzyme A acetyltransferase 1 (acetoacetyl (acetyl-Coenzyme A acetyltransferase 1, acetyl-Coenzyme A 18958 1077 D13921 N Coenzyme A thiolase)) acetyltransferase 1 (acetoacetyl Coenzyme A thiolase)) (acetyl-Coenzyme A acyltransferase 1, acetyl-Coenzyme A (acetyl-Coenzyme A acyltransferase 1, acetyl-Coenzyme A 23699 1139 J02749 N,D,E acyltransferase 1 (peroxisomal 3-oxoacyl-Coenzyme A thiolase)) acyltransferase 1 (peroxisomal 3-oxoacyl-Coenzyme A thiolase)) (acetyl-Coenzyme A dehydrogenase, long-chain, acyl-Coenzyme (acetyl-Coenzyme A dehydrogenase, long-chain, acyl-Coenzyme A 6780 1160 J05029 N A dehydrogenase, long chain) dehydrogenase, long chain) (acetyl-Coenzyme A dehydrogenase, medium chain, acyl-CoA dehydrogenase, acyl-Coenzyme A dehydrogenase, C-4 to C-12 (acetyl-Coenzyme A dehydrogenase, medium chain, acyl-Coenzyme 21078 1143 J02791 N,G straight chain) A dehydrogenase, C-4 to C-12 straight chain) (acidic (leucine-rich) nuclear phosphoprotein 32 family, member 187 1094 D32209 F A, ectodermal) acidic (leucine-rich) nuclear phosphoprotein 32 family, member A (Aconitase, Aconitate hydratase, aconitase 2, mitochondrial, 19991 730 AI103956 K wurfa10e03) aconitase 2, mitochondrial 2098 25 AA799995 C (Actin 5C, actin, beta, actin, beta, cytoplasmic) (actin, beta, actin, beta, cytoplasmic) 21165 78 AA848941 K (actin, alpha 1, alpha actinin, alpha-actinin) actinin, alpha 1 21166 78 AA848941 K (actin, alpha 1, alpha actinin, alpha-actinin) actinin, salpha 1 (activating transcription factor 4, activaling transcription factor 4 (activating transcription factor 4, activating transcription factor 4 (tax- 13633 576 AI012335 M (tax-responsive enhancer element B67)) responsive enhancer element B67)) Table 3 GLGC GenBank Acc or Identifier Seq ID RefSeq ID Model Code Human Homologous Gene Name Human Homologous Cluster Title (activating transcription factor 4, activating transcription factor 4 (activating transcription factor 4, activating transcription factor 4 (tax- 13634 880 AI179381 M (tax-responsive enhancer element B67)) responsive enhancer element B67)) (acyl-CoA dehydrogenase, isovaleryl Coenzyme A (isovaleryl Coenzyme A dehydrogenase, isovaleryl coenzyme A 4449 712 AI102838 N,B,G,K dehydrogenase, isovaleryl coenzyme A dehydrogenase) dehydrogenase) (acyl-CoA dehydrogenase, isovaleryl Coenzyme A (isovaleryl Coenzyme A dehydrogenase, isovaleryl coenzyme A 4450 1161 J05031 N,E dehydrogenase, isovaleryl coenzyme A dehydrogenase) dehydrogenase) (acyl-CoA dehydrogenase, isovaleryl Coenzyme A (isovaleryl Coenzyme A dehydrogenase, isovaleryl coenzyme A 4451 1161 J05031 M,N,F dehydrogenase, isovaleryl coenzyme A dehydrogenase) dehydrogenase) (ACYL-COENZYME A OXIDASE, PEROXISOMAL (EC 1.3.3.6) (PALMITOYL-COA OXIDASE) (AOX), acyl-Coenzyme A oxidase 16150 1 AA799489 G 1, palmitoyl, wu:fb59h12) acyl-Coenzyme A oxidase 1, paimitoyl (ACYL-COENZYME A OXIDASE, PEROXISOMAL (EC 1.3.3.6) (PALMITOYL-COA OXIDASE) (AOX), acyl-Coenzyme A oxidase 16148 1140 J02752 N 1, palmitoyl, wu:fb59h12) acyl-Coenzyme A oxidase 1, palmitoyl (ADP ribosylation factor 51F, ADP-ribosylation factor 6, 21696 346 AA944324 N,C Y116A8C.12.p) ADP-ribosylation factor 6 (alanine-glyoxylate aninotransferase 2, aminotransferase, 7914 439 AB002584 N similar to beta-alanine-pyruvate aminotransferase) alanine-glyoxylate aminotransferase 2 (alanyl (membrane) aminopeptidase, alanyl (membrane) (alanyl (membrane) aminopeptidase, alanyl (membrane) aminopeptidase (aminopeptidase N, aminopeptidase M, aminopeptidawe (aminopeptidase N, aminopeptidase M, microsomal 1540 1246 M25073 N microsomal aminopeptidase, CD13, p150)) aminopeptidase, CD13, p150)) (alcohol dehydrogenase 1 (class 1), alcohol dehydrogenase 1C (alcohol dehydrogenase 1 (class I), alcohol dehydrogenase 1C 22219 1578 X72792 N,F (class I), gamma polypeptide) (class I), gamma polypeptide) (alcohol dehydrogenase; non-specific lipid transfer protein, 25070 1397 S83279 M,N hydroxysteroid (17-beta) dehydrogenase 4) hydroxysteroid (17-beta) dehydrogenase 4 (aldehyde dehydrogenase 3 family, memberA1, aldehyde (aldehyde dehydrogenase 3 family, memberA1, aldehyde 15876 241 AA892582 N,G dehydrogenase family 3, subfamily A1) dehydrogenase family 3, subfamily A1) (aldehyde dehydrogenase 6 family, member A1, aldehyde dehydrogenase family 6, subfamily A1, methylmalonate- (aldehyde dehydrogenase 6 family, member A1, aldehyde 10087 817 AI171803 M semialdehyde dehydrogenase) dehydrogenase family 6, subfamily A1) (aldehyde dehydrogenase 6 family, member A1, aldehyde dehydrogenase family 6, subfamily A1, methylmalonate- (aldehyde dehydrogenase 6 family, member A1, aldehyde 17269 1322 M93401 M semialdehyde dehydrogenase) dehydrogenase family 6, subfamily A1) Table 3 GLGC GenBank Acc or Identifier Seq ID RefSeq ID Model Code Human Homologous Gene Name Human Homologous Cluster Title (aldehyde dehydrogenase, aldehyde dehydrogenase 3 family, (aldehyde dehydrogenase 3 family, member A2, aldehyde 23884 1293 M73714 J member A2, aldehyde dehydrogenase family 3, subfamily A2) dehydrogenase family 3, subfamily A2) (aldehyde dehydrogenase, aldehyde dehydrogenase 9 family, (aldehyde dehydrogenase 9 family, member A1, aldehyde 16885 739 AI105188 K member A1, aldehyde dehydrogenase 9, subfamily A1) dehydrogenase 9, subfamily A1) (aldo0keto reductase family 1, member A1 (aldehyde reductase), (aldo-keto reductase family 1, member A1 (aldehyde reductase), 23109 1072 D10854 N aldo-keto reductase family 1, member A4 (aldehyde reductase)) aldo-keto reductase family 1, member A4 (aldehyde reductase)) (aldo-keto reductase family 7, member A2 (aflatoxin aldehyde (aldo-keto reductase family 7, member A2 (aflatoxin aldehyde reductase), aldo-keto reductase family 7, member A5 (aflatoxin reductase), aldo-keto reductase family 7, member A5 (aflatoxin 23321 252 AA892821 M aldehyde reductase), wu:fb71a02) aldehyde reductase)) (aldo-keto reductase family 7, member A2 (aflatoxin aldehyde (aldo-keto reductase family 7, member A2 (aflatoxin aldehyde reductase), aldo-keto reductase family 7, member A5 (aflatoxin reductase), aldo-keto reductase family 7, member A5 (aflatoxin 23322 252 AA892821 N aldehyde reductase), wu:fb71a02) aldehyde reductase)) (alkaline phosphatase 2, liver, alkaline phosphatase, (alkaline phosphatase 2, liver, alkaline phosphatase, 14997 1150 J03572 N liver/bone/kidney) liver/bone/kidney) (alkaline phosphatase 2, liver, alkaline phosphatase, (alkaline phosphatase 2, liver, alkaline phosphatase, 14996 1526 X16038 M,D liver/bone/kidney) liver/bone/kidney) 16268 1419 U10894 N (allograft inflammatory factor 1, sb:cb10) allograft inflammatory factor 1 (alpha Spectrin, sp;ectrin alpha 2, spectrin, alpha, non- 20741 510 AF084186 A,J erythrocytic 1 (alpha-fodrin)) (spectrin alpha 2, spectrin, alpha, non-erythrocytic 1 (alpha-fodrin)) (alpha-N-acetylgalactosaminide alpha-2,6-sialytransferase III, (alpha-N-acetylgalaclosaminide alpha-2,6-sialyltransferase III, sialyltransferase 7 ((alpha-N-acetylneuraminyl 2,3-betagatactosyl-sialyltransferase 7 ((alpha-N-acetylneuraminyl 2,3-betagalactosyl- 17196 942 AI231519 M,N,I 1,3)-N-acetyl galactosaminide alpha-2,6-sialyltransferase) C) 1,3)-N-acetyl galactosaminide alpha-2,3-sialyltransferase) C) (aminoadipate aminotransferase, kynurenine aminotransferase (L-kynurenine/alpha-aminoadipate aminotransferase, kynurenine 1542 1614 Z50144 N,J II) aminotransferase II) (aminolevulinate, delta-, synthase 2 (sideroblastic/hypochromic (aminolevulinate, delta-, synthase 2 (siderob/astic/hypochronic 16448 1117 D86297 N anemia), aminclevulinic acid synthase 1) anemia), aminolevulinic acid synthase 1) 2079 1189 L14462 F (amino-terminal enhancer of split, chico) amino-terminal enhancer of split (amphiphysin, amphiphysin (Stiff-Man syndrome with brease (amphiphysin, amphiphysin (Stiff-Man syndrome with breast cancer 5329 646 AI045970 M cancer 128kDa autoantigen)) 128kDa autoantigen)) Table 3 GLGC GenBank Acc or Identifier Seq ID RefSeq ID Model Code Human Homologous Gene Name Human Homologous Cluster Title 21391 600 AI013902 M,K (Annexin X, annexin A7) annexin A7 (APEX nuclease (multifunctional DNA repair enzyme) 1, (APEX nuclease (multifunctional DNA repair enzyme) 1, 20801 1104 D44495 M,N,H,I,J,L apurinic/apyrimidinic endonuclease 1, hm.zehn1532) apurinic/apyrimidinic endonuclease 1) 1419 1492 U90887 N (arginase type II, arginase, type II, wu:fb67g02) 9arginase type II, arginase, type II) 4467 1274 M57664 N (Arginine kinase, arginine kinase, creatine kinase, brain) creatine kinase, brain (arginine vasopressin receptor 2, arginine vasopressin receptor 2 (arginine vasopressin receptor 2, arginine vasopressin receptor 2 20173 1605 Z11932 N,C (nephrogenic diabeles insipidus)) (nephrogenic diabetes insipidus)) (argininosuccinate lyase, hyterogeneous nuclear (argininosuccinale lyase, heterogeneous nuclear ribonucleoprotein 4234 457 AB016536 N,K ribonucleoprotein A/B) A/B) 20597 1512 X12459 n (argininosuccinate synthetase, argininosuccinale synthetase 1) (arginosuccinate synthetase, argininosuccinate synthetase 1) (Aspartate aminotransferase, glutamate oxaloacetate (glutamate oxaloacetate transaminase 2, mitochondrial, glutamic- transaminase 2, mitochondrial, glutamic-oxaloacetic oxaloacetic transaminase 2, mitochondrial (aspartate 17630 201 AA892012 N transaminase 2, mitochondrial (aspartate aminotransferase 2)) aminotransferase 2)) (aspartoacylase (aminoacylase 2, Canavan disease), (aspartoacylase (aminoacylase 2, Canavan disease), 10789 947 AI232059 M aspartoacylase (aminoacylase) 2) aspartoacylase (aminoacylase) 2) (ATP synthase, H+ transporting, mitochondrial F0 complex, (ATP synthase, H+ transporting, mitochondrial F0 complex, subunit subunit F, ATP synthase, H+ transporting, mitochondrial F0 F, ATP synthase, H+ transporting, mitochondrial F0 complex, 20725 1541 X54510 A complex, subunit F6) subunit F6) (ATP synthase, H+ transporting, mitochondrial F1 complex, delta (ATP synthase, H+ transporting, mitochondrial F0 complex, subunit subunit F, ATP synthase, H+ transporting, mitochondrial F0 F, ATP synthase, H+ transporting, mitochondrial F0 complex, 20725 1541 X54510 A complex, subunit F6) subunit F6) (ATP synthase, H+ transporting, mitochondrial F1 complex, delta (ATP synthase, H+ transporting, mitochondrial F1 complex, delta 18449 1399 U00926 H subunit, RIKEN cDNA 0610008F14 gene) subunit, RIKEN cDNA 0610008F14 gene) (ATPase, Ca++ transporting, cardiac muscle, slow twitch 2, 12349 5 AA799276 M Calcium ATPase at 60A, E1-E2 ATPases) ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 (ATPase, H+ transporting, cardiac mnuscle, slow twitch 2, 12349 5 AA799276 M Calcium ATPase at 60A, E1-E2 ATPases) ATPase, Ca++ transporting, cardiac muscle, slow twitch 2 (ATPase, H+ transporting, lysosomal V0 subunit a isoform 1, CLATHRIN-COATED VESICLE/SYNAPTIC VESICLE PROTON 20841 1279 M58758 H PUMP 116 KD SUBUNIT (EC 3.6.1.34)) ATPase, H+ transporting, lysosomal V0 subunit a sioform 1 (ATPase, Na+/K+ transporting, beta 1 polypeptide, ATPase, 23708 1335 NM_013113 N Na+/K+ transporting beta 1a polypeptide) ATPase, Na+/K+ transporting, beta 1 polypeptide (ATPase, Na+/K+ transporting, beta 1 polypeptide, ATPase, Na+/K+ transporting, beta 1a polypeptide, non-metastatic cells 7, protein expressed in, non-metastatic cells 7, protein expressed in (ATPase, Na+/K+ transporting, beta 1 polypeptide, non-metastatic (nucleoside-diphosphate kinase), nucleoside diphosphate kinase cells 7, protein expressed in, non-metastatic cells 7, protein 23709 1356 NM_138532 N Z4) expressed in (nucleoside-diphosphate kinase)) Table 3 GLGC Genbank Acc or Identifier Seq ID RefSeq ID Model Code Human Homologous Gene Name Human Homologous Cluster Title (ATP-binding cassetle, sub-family B (MDR/TAP), member 1, ATP-binding cassette, sub-family B (MDR/TAP), member 1A, (ATP-binding cassette, sub-family B (MDR/ATP), member 1, ATP- ATP-binding cassette, sub-family B (MDR/TAP), member 1B, binding cassette, sub-family B (MDR/TAP), member 1A, ATP- 5733 1303 M81855 N Multi drug resistance 49) binding cassette, sub-family B (MDR/TAP), member 1B) (Bardet-Biedl syndrome 2, Baret-Biedl syndrome 2 homolog (Bardet-Biedl syndrome 2, Bardet-Biedl syndrome 2 homolog 5565 362 AA945879 M,C (human)) (human)) (basic transcription element binding protein 1, similar to Kruppel- 8640 1073 D12769 D like factor 9, wu:fi22b08) basic transcription element binding protein 1 (B-cell receptor-associated protein 37, Prohibitin, repressor of (B-cell receptor-associated protein 37, repressor of estrogen 16398 1478 U75392 N estrogen receptor activity) receptor activity) (B-cell translocation gene 1, anti-proliferative, similar to B-cell 19 1197 L26268 M translocation gene 1, anti-proliferative) B-cell translocation gene 1, anti-proliferative (B-cell translocation gene 2, anti-proliferative, BTG family, (B-cell translocation gene 2, anti-prlliferative, BTG family, member 15300 1283 M60921 M member 2) 2) (B-cell translocation gene 2, anti-proliferative, BTG family, (B-cell translocation gene 2, anti-prliferative, BTG family, member 15299 1340 NM_017259 M,I,J member 2) 2) 23679 511 AF087037 C,L (B-cell translocation gene 3, BTG family, member 3) (B-cell translocation gene 3, BTG family, member 3) (BCL2/adenovirus E1B 19dDa interacting protein 3-like, (BCL2/adenovirus E1B 19kDa interacting protein 3-like, 912 1468 U59184 N associated X protein) (BCL2-associated X protein, Bcl2-associated X protein) (beta integrin, integrin beta 1 (fibronectin receptor beta), integrin, (integrin beta 1 (fibronectin receptor beta), integrin, beta 1 beta 1 (fibronectin receptor, beta polypeptide, anligen CD29 (fibronectin receptor, beta polypeptide, antigen CD29 includes 14989 857 Al177366 M,K includes MDF2, MSK12), myospheroid) MDF2, MSK12)) 1508 1332 M97662 N,G (beta-ureidopropionase (rat), ureidopropionase, beta) ureidopropionase, beta 19824 1125 E13557 N,G,K (black, cysteine sulfinic acid decarboxylase) cysteine sulfinic acid decarboxylase 19825 1288 M64755 N (black, cysteine sulfinic acid decarboxylase) cysteine sulfinic acid decarboxylase (brain protein 44-like, similar to apoplosis-regulating basic 17887 830 Al172414 J protein) brain protein 44-like 18503 783 Al169021 G (calbindin 1, 28kDa, calbindin-28K) (calbindin 1,28kDa, calbindin-28K) 18501 1254 M31178 N (calbindin 1, 28kDa, calbindin-28K) (calbindin 1,28kDa, calbindin-28K) 18502 1254 M31178 N (calbindin 1, 28kDa, calbindin-28K) (calbindin 1,28kDa, calbindin-28K) Table GLGC GenBank Acc or Identifier Seq ID RefSeq ID Model Code Human Homologous Gene Name Human Homologous Cluster Title (calcium regulated heat stable protein 1, calcium regulated heat (calcium regulated heat stable protein 1, calcium regulated heat 15132 936 Al231180 G stable protein 1,24kDa) stable protein 1,24kDa) (calmodulin 2 (phosphorylase kinase, delta), similar to 20809 1229 M17069 N.D Calmodulin CMD-1 (16.8 kD) (cmd-1), wu:fb69c08) calmodulin 2 (phophorylase kinase, delta) (Calmodulin, calmodulin 1, calmodulin 1 (phosphorylase kinase, 25802 1353 NM_031969 G,K delta)) (calmodulin 1, calmodulin 1 (phosphorylase kinase, delta)) (calmodulin, calmodulin 3, calmodulin 3 (phosphorylase kinase, 20518 1520 X14265 N delta)) (calmodulin3 , calmodulin 3 (phosphorylase kinase, delta)) 15035 1472 U62897 B (carboxypeptidase, carboxypeptidase D, silver) carboxypeptidase D (camitine palmiloyltransferase 1, liver, camitine palmitoyltransferase 1A (liver), mitochondrial camiline (carnitine palmitoyltransferase 1, liver, carnitine palmitoyltransterase 15411 1178 L07736 N,B,L palmitoyltransferase l) 1A (liver)) (carnitine palmitoyltransferase 2, camitine palmiloyltransferase II, 1977 1164 J05470 N,L wu:fa03e08) (carnitine palmitoyltransferase 2, camitine palmitoyltransferase II) 16116 475 AF025670 F (caspase 6, caspase 6, apoptsis-related cysteine protease) (caspase 6, caspase 6, apoptosis-related cysteine protease) 15741 1214 M11670 N (Catalase, catalase) catalase 1462 999 Al235585 M,E,G (cathepsin D, cathepsin D (lysosomal aspartyl protease) (cathepsin D, cathepsin D (lysosomal aspartyl protease)) 1463 1540 X54467 M,G,K (cathepsin D, cathepsin D (lysosomal aspartyl protease)) (cathepsin D, cathepsin D (lysosomal aspartyl protease)) (CD24a antigen, hypothelical gene supported by NM_013230; (CD24a antigen, hypothelical gene supported by NM_013230; 20828 814 Al171462 M,E,K AK026603; X69397; BC007674; D87667; M58664; S75311) AK026603; X69397; BC007674; D87667; M58664; S75311) (CD24a antigen, hypothetical gene supported by NM_013230; (CD24a antigen, hypothetical gene supported by NM_013230; 20829 1457 U49062 M,D AK026603; X69397; BC007674; D87667; M58664; S75311) AK026603; X69397; BC007674; D87667; M58664; S75311) (CD24a antigen, hypothetical gene supported by NM_013230; (CD24a antigen, hypothetical gene supported by NM_013230; 20830 1457 U49062 M AK026603; X69397; BC007674; D87667; M58664; S75311) AK026603; X69397; BC007674; D87667; M58664; S75311) (CD99 antigen-lie 2, MIC2 (monoclonal Imperial Cancer (CD99 antigen-lie 2, MIC2 (monocional Imperial Cancer Research 9332 952 Al232210 F Research Fund 2)-like 1) Fund 2)-like 1) (cdc2, cell division cycle 2 homolog A (S. pombe), cell division (cell division cycle 2 homolog A (S. pombe), cell division cycle 2, G1 21651 1560 X60767 N,E cycle 2, G1 to S and G2 to M) to S and G2 to M) (cellular myelocytomatosis oncogene, myelocytomatosis oncogene, v-myc myelocytomatosis viral oncogene homolog (myelocytomatosis oncogene, v-myc myelocytomatosis viral 2629 1598 Y00396 K (avian)) oncogene homolog (avian)) (cellular nucleic acid binding protein, zinc finger protein 9 (a (cellular nucleic acid binding protein, zinc finger protein 9 (a cellular 20960 1106 D45254 D cellular retroviral nucleic acid binding protein)) retroviral nucleic acid binding protein)) Table 3 GLGC GenBank Acc or Identifier Seq ID RefSeq ID Model Code Human Homologous Gene Name Human Homologous Cluster Title (ceroid-lipofuscinosis, neuronal 2, ceroid-lipofusionosis, neuronal (ceroid-lipofuscinosis, neuronal 2, ceroid-lipofuscinosis, neuronal 2, 19936 385 AA956517 D 2, late infantile (Jansky-Bielschowsky disease), wu:fa01b09) late infantile (Jansky-Bielschowsky disease)) (ceroid-lipofuscinosis, neuronal 2, ceroid-lipofuscinosis, neuronal (ceroid-lipofuscinosis, neuronal 2, ceroid-lipofuscinosis, neuronal 2, 11429 798 Al169706 H 2, late infantile (Jansky-Bielschowsky disease), wu:fa01b09 late infantile (Jansky-Bielschowsky diseas)) 16521 557 Al010470 B,J,L (ceruloplasmin, ceruloplasmin (ferroxidase)) (ceruloplasmin, ceruloplasmin (ferroxidase)) 16520 1204 L33869 M,B,C,L (ceruloplasmin, ceruloplasmin (ferroxidase)) (ceruloplasmin, ceruloplasmin (ferroxidase)) (chemokine (C-X-C motif) ligand 12, chemokine (C-X-C motif) (chemokine (C-X-C motif) ligand 12, chemokine (C-X-C motif) ligand 4330 60 AA818747 M,B ligand 12 (stromal cell-derived factor 1)) 12 (stromal cell-derived factor 1)) (chemokine (C-X-C motif) ligand 12, chemokine (C-X-C motif) (chemokine (C-X-C motif) ligand 12, chemokien (C-X-C motif) ligand 24321 956 Al232340 M,K,L ligand 12 (stromal cell-derived factor 1)) 12 (stromal cell-derived factor 1)) (Chromatin assembly factor 1 subunit, retinoblastoma binding 17535 513 AF090306 N,E protein 7) retinoblastoma binding protein 7 (chromosome 12 open reading frame 8, endoplasmic reticulum (chromosome 12 open reading frame 8, endoplasmic reticulum 16552 1449 U36482 L protein 29) protein 29) Clathrin coat assembly protein, adaptor-related protein complex 20682 1482 U75917 B 2, sigma 1 subunit, similar to clathrin-associated protein 17 - rat) adaptor-related protein complex 2, sigma 1 subunit (clathrin, light polypeptide (Lcb), similar to Clathrin light chain B 17154 1228 M15883 J (Lcb)) clathrin, light polypeptide (Lcb) (clusterin, clusterin (complement) lysis inhibitor, SP-40,40, (clusterin, clusterin (complement lysis inhibitor, SP-40,40, sulfated sulfated glycoprotein 2, testosterone-repressed prostate glycoprotein 2, testosterone-repressed prostate message 2, 7101 1287 M64733 M,E message 2, apolipoprotein J)) apolipoprotein J)) (coagulation factor III, coagulation factor III (thromboplastin, (coagulation factor III, coagulation factor III (thromboplastin, tissue 24874 1410 U07619 N tissue factor}) factor}) 15364 742 Al105348 J (cofilin 1 (non-muscle), similar to cofilin 1, non-muscle) cofilin 1 (non-muscle) 16610 1091 D28557 N,E,L (cold shock domain protein A, ypsilon schachtel) cold shock domain protein A (Collapsin Response Mediator Protein, Ulip like protein, 811 1110 D63704 M,I dihydropyrimidinase) dihydropyrimidinase (Collapsin Response Mediator Protein, Ulip like protein, 812 1110 D63704 M,I dihydropyrimidinase) dihydropyrimidinase Table 3 GLGC GenBank Acc or Identifier Seq ID RefSeq ID Model Code Human Homologous Gene Name Human Homologous Cluster Title (complement component 4 (within H-2S), complement (complement component 4 (within H-2S), complement component 15851 1453 U42719 M component 4B) 4B) (connexin 43, gap junction membrane channel protein alpha 1, (gap junction membrane channel protein alpha 1, gap junction 15393 806 Al170663 J gap junction protein, alpha 1,43kDa (connexin 43)) protein, alpha 1,43kDa (connexin 43)) (coracle, erythrocyte membrane protein band 4.1-like 1, erythrocyte membrane protein band 4.1-like 3, erythrocyte (erythrocyte membrane protein band 4.1-like 1, erythrocyte protein 3125 934 Al231028 K protein band 4.1-like 1) band 4.1-like 1) 1727 461 AF001417 M (core promoter element binding protein, zinc finger protein) core promoter element binding protein (coronin, actin binding protein 1A, coronin, actin binding protein, 21695 231 AA892506 N,G 1A) (coronin, actin binding protein 1A, coronin, actin binding protein, 1A) (Cortactin, cortactin, ems1 sequence (mammary tumor and (cortactin, ems1 sequence (mammary tumor and squamous cell 19058 493 AF054618 E squamous cell carcinoma-associated (p80/85 src substrate)) carcinoma-associated (p80/85 src substrate)) 13723 1272 M55534 N,K (crystallin, alpha A, crystallin, alpha B) crystallin, alpha B (cubilin (intrinsic factor-cobalamin receptor), similar to cubilin; 16407 471 AF022247 N cubilin (intrinsic factor-cobalamin receptor)) cubilin (intrinsic factor-cobalamin receptor) (Cu-Zn superoxide dismutase, similar to superoxide dismutase 1, soluble, superoxide dismutase 1, soluble (amyotrophic lateral superoxide dismutase 1, soluble (amyotrophic lateral sclerosis 1 20876 1238 M21060 J sclerosis 1 (adult))) (adult)) 11434 1079 D14014 N,B (cyclin D1, cyclin D1 (PRAD1: parathyroid adenomatosis 1)) (cyclin D1, cyclin D1 (PRAD1:parathyroid adenomatosis 1)) 24232 1359 NM_171992 B (cyclin D1, cyclin D1 (PRAD1: parathyroid adenomatosis 1)) (cyclin D1, cyclin D1 (PRAD1: parathyroid adenomatosis 1)) (cyclin-dependent kinase inhibitor 1A (P21), cyclin-dependent (cyclin-dependent kinase inhibitor 1A (P21), cyclin-dependent kinase 133 1436 U24174 N kinase inhibitor 1A (p21, Cip1)) inhibitor 1A (p21, Cip1)) (cystathionase (cystathionine gamma-lyase), cystathionine 18452 1085 D17370 M,N gamma-lyase, wu:fb48e03) cystathionase (cystathionine gamma-lyase) (cystathionase (cystathionine gamma-lyase), cystathionine 18453 1085 D17370 N,G gamma-lyase, wu:fb48e03) cystathionase (cystathionine gamma-lyase) (cystathionine beta-synthase, cystathionine-beta-synthase, 291 1316 M88347 M,N,F wu:fq06c06) (cystathionine beta-synthase, cystathionine-beta-synthase) 13392 982 Al234146 M (cysteine and glycine-rich protein 1, cysteine rich protein 1) (cysteine and glycine-rich protein 1, cysteine rich protein 1) (Cysteine proteinase-1, cathepsin L, cathepsin L2, cathepsin-like 3431 846 Al176595 N protease, hatching gland gene 1) (cathepsin L, cathepsin L2) 19543 1455 U44948 N (cysteine rich protein 2, cysteine-rich protein 2) (cysteine rich protein 2, cysteine-rich protein 2) Table 3 GLGC GenBank Acc or Identifier Seq ID RefSeq ID Model Code Human Homologous Gene Name Human Homologous Cluster Title (cytochrome c oxidase subunit Vlc, cytochrome c oxidase, (cytochrome x oxidase subunit Vlc, cylochrome c oxidase, subunit 23225 1249 M27467 N subunit Vlc) Vlc) (Cytochrome P450 reductase, NADPH-cytochrome P450, P450 1921 1123 E01524 N (cytochrome) oxidoreductase P450 (cytochrome) oxidoreductase (Cytochrome P453 reduclase, NADPH-cytochrome P450, P450 1920 1213 M10068 N (cytochrome) oxidoreductase) P450 (cytochrome) oxidoreductase (cytochrome P450, family 2, subfamily E, polypeptide 1, (cytochrome P450, family 2, subfamily E, polypeptide 1, cytochrome 4011 496 AF056333 N,J cytochrome P450, family 2, subfamily e, polypeptide 1) P450, family 2, subfamily e, polypeptide 1) (cytochrome P450, family 2, subfamily E, polypeptide 1, (cytochrome P450, familhy 2, subfamily E, polypeptide 1, cytochrome 4012 1367 S48325 N,J cytochrome P450, family 2, subfamily e, polypeptide 1) P450, family 2, subfamily e, polypeptide 1) (cytochrome P450, family 4, subfamily A, polypeptide 11, (cytochrome P450, family 4, subfamily A, polypeptide 11, 67 1268 M37828 B cytochrome P450, family 4, subfamily a, polypeptide 12) cytochrome P450, family 4, subfamily a, polypeptide 12) (cytochrome P450, family 4, subfamily F, polypeptide 2, (cytochrome P450, family 4, subfamily F, polypeptide 2, cytochrome 20716 1323 M94548 G cytochrome P450, family 4, subfamily f, polypeptide 14) P450, family 4, subfamily f, polypeptide 14) (Cytoplasmic dynein light chain 2, dynein, cytoplasmic, light (dynein, cytoplasmic, light chain 1, dynein, cytoplasmic, light 17473 544 Al009806 M,N,K chain 1, dynein, cytoplasmic, light polypeptide 1) polypeptide 1) (D site albumin promoter binding protein, D site of albumin (D site albumin promoter binding protein, D site of albumin promoter 1762 1147 J03179 N promoter (albumin D-box) binding protein) (albumin D-box) binding protein) (D site albumin promoter binding protein, D site of albumin (D site albumin promoter binding protein, D site of albumin promoter 1763 1147 J03179 N promoter (albumin D-box) binding protein) (albumin D-box) binding protein) (D-3-Phosphoglycerate dehydrogenase, phosphoglycerate dehydrogenase, similar to D-3-phosphoglycerate dehydrogenase 21587 293 AA899141 D (3-PGDH)) phosphoglycerate dehydrogenase (D-3-Phosphoglycerate dehydrogenase, phosphoglycerate dehydrogenase, similar to D-3-phosphoglycerate dehydrogenase 21585 1596 X97772 D (3-PGDH)) phosphoglycerate dehydrogenase (D-3-Phosphoglycerate dehydrogenase, phosphoglycerate dehydrogenase, similar to D-3-phosphoglycerate dehydrogenase 21586 1596 X97772 D (3-PGDH)) phosphoglycerate dehydrogenase (DEAD (Asp-Glu-Ala-Asp) box polypeptide 39, DEAD/H (Asp-Glu- 4327 501 AF063447 M,G,I (DEAD (Asp-Glu-Ala-Asp) box polypeptide 39, Helicase at 25E) Ala-Asp/His) box polypeptide 39) 12422 1053 AJ006971 N (death-associated kinase 3, death-associated protein kinase 3) (death-associated kinase 3, death-associated kinase 3, death-associated protein kinase 3) 12423 1053 AJ006971 N (death-associated kinase 3, death-associated protein kinase 3) (death-associated kinase 3, death-associated kinase 3, death-associated protein kinase 3) Table 3 GLGC GenBank Acc or Identifier Seq ID Ref Seq ID Model Code Human Homologus Gene Name Human Homologous Cluster Title (diacylglycerol kinase, gamma, diacylglycerol kinase, gamma (diacylglycerol kinase, gamma, diacylglycerol kinase, gamma 755 1100 D38448 M,N 90kDa) 90kDa) (diacylglycerol kinase, gamma, diacylglycerol kinase, gamma (diacylglycerol kinase, gamma, diacylglycerol kinase, gamma 754 1336 NM_013126 N 90kDa) 90kDa) (Dihydropteridine reductase, quininoid dihydropteridine (quininoid dihydropteridine reductase, quinoid dihydropteridine 13479 1149 J03481 N reductase, quinoid dihydropteridine reductase reductase) (Dihydropteridine reductase, quininoid dihydropteridine (quininoid dihydropteridine reductase, quinoid dihydropteridine 13480 1149 J03481 N reductase, quinoid dihydropteridine reductase) reductase) (dipeptidylpeptidase 4, dipeptidylpeptidase 4 (CD26, adenosine (dipeptidlpeptidase 4, dipeptidylpeptidase 4 (CD26, adenosine 7784 1157 J04591 M,N,I deaminase complexing protein 2)) deaminase complexing protein 2)) (disabled homolog 2 (Drosophila), disabled homolog 2, mitogen- (disabled homolog 2 (Drosophila), disabled homolog 2, milogen- 4504 1495 U95178 D responsive phosphoprotein (Drosophila)) responsive phosphoprotein (Drosophila) 25247 1054 AJ011608 N (DNA primase, p49 subunit, primase, polypeptide 1,49kDa) (DNA primase, p49 subunit, primase, polypeptide 1,49kDa) 23718 381 AA955790 A (DNA segment, Chr 3, MJeffers 1, NRAS-related gene) (DNA segment, Chr 3, MJeffers 1, NRAS-related gene) (DNA topoisomerase II, Toposiomerse 2, topoisomerase (DNA) (topoisomerase (DNA) II alpha, topoisomerase (DNA) II alpha 23778 298 AA899854 N,E II alpha, topoisomerase (DNA) II alpha 170kDa) 170kDa) (DNA topoisomerase II, Topoisomerase 2, topoisomerase (DNA) (topoisomerase (DNA) II alpha, topoisomerase (DNA) II alpha 23780 1608 Z19552 E II alpha, topoisomerase (DNA) II alpha 170kDa) 170kDa) (DNA-damage inducible transcript 3, DNA-damage-inducible (DNA-damage inducible transcript 3, DNA-damage-inducible 1598 1445 U30186 N transcript 3) transcript 3) (Dodeca-satellite-binding protein 1, high density lipoprotein 23282 1491 U90725 A binding protein (vigilin), high-density lipoprotein-binding protein) high density lipoprotein binding protein (vigilin) (dodecenoyl-Coenzyme A delta isomerase (3,2 trans-enoyl- (dodecenoyl-Coenzyme A delta isomerase (3,2 trans-enoyl- Coenyme A isomerase), dodecenoyl-Coenzyme A delta Coenzyme A isomerase), dodecenoyl-Coenzyme A delta isomerase 18687 804 Al170568 N isomerase (3,2 trans-enoyl-Coenzyme A isomerase)) (3,2 trans-enoyl-Coenzyme A isomerase)) (dodecenoyl-Coenzyme A delta isomerase (3,2 trans-enoyl- (dodecenoyl-Coenzyme A delta isomerase (3,2 trans-enoyl- Coenyme A isomerase), dodecenoyl-Coenzyme A delta Coenyme A isomerase), dodecenoyl-Coenzyme A delta isomerase 18686 1062 D00729 N isomerase (3,2 trans-enoyl-Coenzyme A isomerase)) (3,2 trans-enoyl-Coenzyme A isomerase)) (Dopa decarboxylase, aromatic-L-amino-acid decarboxylase, dopa decarboxylase, dopa decarboxylase (aromatic L-amino (dopa decarboxylase, dopa decarboxylase (aromatic L-amino acid 1431 632 Al044610 0 acid decarboxylase)) decarboxylase)) Table 3 GLGC GenBank Acc or Identifier Seq ID Refseq ID Model Code Human Homologous Gene Name Human Homologous cluster Title (Dopa decarboxylase, aromatic-L-amino-acid decarboxylase, dopa decarboxylase, dopa decarboxylase (aromatic L-amino (dopa decarboxylase, dopa decarboxylase (aromatic L-amino acid 1430 1309 M84648 M acid decarboxylase)) decarboxylase)) (dual specificity phosphatase 5, similar to MAP-kinase 1183 465 AF013144 N phosphatase (cpg21)) dual specificity phosphatase 5 (dUTP pyrophosphatase, deoxyuridine 5'-triphosphate 20896 1475 U64030 A.F nucleotidchydrolase, deoxyuridine triphosphatase) (dUTP pyrophosphatase, deoxyuridine triphosphatase) (Dynein light chain 90F, t-complex testis expressed 1, t-complex- (t-complex lestis expressed 1,1-complex-associated-testis- 15662 445 AB010119 N.G associated-testis-expressed 1-like 1) expressed 1-like 1) (Dynein light chain 90F, t-complex testis expressed 1, t-complex- (t-complex testis expressed 1, t-complex-associated-testis- 15663 834 Al175566 M associated-testis-expressed 1-like 1) expressed 1-like 1) 9176 691 Al072675 A (dystonia 1, dystonia 1, torsion (autosomal domainant; torsin A)) (dystonia 1, dystonia 1, torsion (autosomal dominant; torsin A)) (Ecdysone receptor, nuclear receptor subfamily 1, group H, 19712 1429 U18374 K member 4) nuclear receptor subfamily 1, group H, member 4 (Ecdysone receptor, nuclear receptor subfamily 1, group H, member 4, solute carrier family 2 (facilitated glucose (nuclear receptor subfamily 1, group H, member 4, solute carrier transporter), member 5, solute carrier family 2 (facilitated family 2 (faciliated glucose transporter), member 5, solute carrier 1214 1076 D13871 M,N,K glucose/fructose transporter), member 5) family 2 (facilitated glucose/fructose transporter), member 5) (Ecdysone-inducible gene L3, lactate dehydrogenase 2, B chain, 7124 1409 U07181 E lactate dehydrogenase B, Lactate dehydrogenase B4) (lactate dehydrogenase 2, B chain, lactate dehydrogenase B) (Elongation factor 2b, Elongation factor tu family (contains ATP/GTP binding P-loop), eukaryclic translation elongation 17563 875 Al178750 N factor 2) eukaryotic translation elongation factor 2 (enoyl Coenzyme A hydratase 1, peroxisomal, enoyl coenzyme (enoyl Coenzyme Ahydratase 1, peroxisomal, enoyl coenzyme A 20925 1412 u08976 n.l A hydratase 1, perxisomal) hydratase 1, peroxisomal) 23194 227 AA892417 M (ephrin A1, ephrin-A1) (ephrin A1, ephrin-A1) (epidermal growth factor receptor, epidermal growth factor receptor (erythroblastic leukemia viral (v-erb-b) on cogene (epidemal growth factor receptor, epidermal growth factor receptor 17907 969 Al233224 M homolog, avian)) (erythroblastic leukemia viral (v-erb-b) oncogene homolog, avian)) (epidermal growth factor, epidermal growth factor (beta- (epidermal growth factor, epidermal growth factor (beta- 20885 1403 U04842 N,G,K urogastrone)) urogastrone)) (epidermal growth factor, epidermal growth factor (beta- (epidermal growth factor, epidermal growth factor (beta- 20884 1513 X12748 N,G,K urogastrone)) urogastrone)) Table 3 GLGC GenBank Acc or identifier Seq ID RefSeq ID Model Code Human Homologous Gene Name Human Homologous Cluster Title 21509 98 AA851618 G (epithelial membrane protein 3, wu:fa04d03) epithelial membrane protein 3 (epoxide hydrolase, epoxide hydroclase 1, microsomal, epoxide (epoxide hydrolase 1, microsomal, epoxide hydrolase 1, microsomal 17541 1247 M26125 M,N,A,B,H,I hydrolase 1, microsomal (xenobiotic) (xenobiotic) (erythrocyte membrane protein band 4.1-like 3, erythrocyte (erythrocyte membrane protein band 4.1-like 3, erythrocyte protein 8188 652 Al058943 M protein band 4.1-like 3) band 4.1-like 3) 744 506 AF076856 M,N (espin, forked) espin (eukaryotic translation initiation factor 2, subunit 1 alpha, (eukaryolic translation initiation factor 2, subunit 1 alpha, eukaryotic 4592 1135 J02646 H eukaryotic translation initiation factor 2, subunit 1 alpha, 35kDa) translation initiation factor 2, subunit 1 alpha, 35kDa) (eukaryotic translation initiation factor 4E, eukaryclic translation initiation factor elF4E-1, similar to Eukaryotic translation initiation (eukaryotic translation initiation factor 4E, similar to Eukaryotic factor 4E (eIF-4E) (eIF-4E) (mRNA cap-binding protein) (eIF-4F translation initiation factor 4E (eIF-4E) (eIF-4E) (mRNA cap-binding 1764 1591 X83399 C 25 kDa subunit), translation initiation factor) protein) (eIF-4F 25 kDa subunit) (Excitatory amino acid transporter 1, solule carrier family 1 (solute carrier family 1 (neuronal/epithelial high affinity glulamate (neuronal/epithelial high affinity glutamate transporter, system transporter, system Xag), member 1, solute carrier family 1, member 21147 1111 D63772 M,F,H,I,J,L Xag), member 1, solute carrier family 1, member 1) 1) (Excitatory amino acid transporter 1, solute carrier family 1 (solute carrier family 1 (neuronal/epithelial high affinity gluamate (neuronal/epithelial high affinity glutamate transporter, system transporter, system Xag), member 1, solute carrier family 1, member 21145 1334 NM_013032 M,B Xag), member 1, solute carrier family 1, member 1) 1) (expressed sequence AW261723, solute carrier family 17 (expressed sequence AW261723, wolule carrier family 17 (sodium 5920 788 Al169163 B (sodium phosphate), member 3) phsophate), member 3) (famesyl diphosphate famesyl transferase 1, famesyl- (famesyl diphosphate famesyl transferase 1, famesyl-diphosphate 16449 1327 M95591 N diphosphate famesyltransferase 1) farnesyltransferase 1) (famesyl diphosphate famesyl transferase 1, famesyl- (famesyl diphosphate famesyl transferase 1, famesyl-diphosphate 16450 1327 M95591 N diphosphate famesyltransferase 1) famesyltrarnsferase 1) (famesyl diphosphate synthase (famesyl pyrophosphate (famesyl diphosphate synthase (famesyl pyrophosphate synthelase, synthetase, dimethylallyltranstransferase, dimethylallyltranstransferase, geranyltranstransferase), famesyl 15069 1319 M89945 H geranyltranstrarnsferase), famesyl diphosphate synthetase) diphosphate synthetase) (farnesyl diphosphate synthase (famesyl pyrophosphate (famesyl diphosphate synthase (famesyl pyrophosphate synthe5tase, synthetase, dimethylallyltranstransferase, dimethylalyltransferase, geranyltrarnstransferase), famesyl 25460 1319 M89945 N geranyltranstrarnsferase), famesyl diphosphate synthetase) diphosphate synthetase) (fatty acid briding protein 11, oocyte, fatty acid binding protein 3, muscle and heart, fatty acid binding protein 3, muscle and heart (fatty acid binding protein 3, muscle and heart, fatty acid binding 16476 1141 J02773 M,L (mammary-derived growth inhibitor)) protein 3, muscle and heart (mammary-derived growth inhibitor)) Table 3 GLGC GenBank Acc or Identifier Seq ID RelSeq ID Model Code Human Homologous Gene Name Human Homologous Cluster Tille (fatty acid Coenzyme a ligase, long chain 2, fatly-acid- (fatty acid Coenzyme A ligase, long chain 2, fatty-acid-Coenzyme A 20983 634 AI044900 K Coenzyme A ligase, long-chain 2) ligase, long-chain 2) (fatty acid Coenzyme a ligase, long chain 5, fatly-acid- (fatty acid Coenzyme A ligase, long chain 5, fatty-acid-Coenzyme A 15926 451 AB012933 D Coenzyme A ligase, long-chain 5, wu:fa04h02) (fatty acid-coenzyme A ligase, long chin 4, fatty-acid- Coenzyme A ligase, long-chain 4, long-chain-fatty-acid coA (fatty acid-coenzyme A ligase, long chin 4, fatty-acid--Coenzyme A 13004 1007 AI236284 J,L ligase) ligase, long-chain 4) (fatty acid-coenzyme A ligase, long chin 4, fatty-acid- Coenzyme A ligase, long-chain 4, long-chain-fatty-acid coA (fatty acid-coenzyme A ligase, long chin 4, fatty-acid--Coenzyme A 13005 1116 D85189 N,C ligase) ligase, long-chain 4) (Fc fragment of IgG, low affinity IIa, receptor for (CD32), Fc (Fc fragment of IgG, low affinity IIa, receptor for (CD32), Fc receptor, 20868 1256 M32062 N receptor, IgG, low affinity III) IgG, low affinity III) (Fc fragment of IgG, low affinity IIa, receptor for (CD32), Fc (Fc fragment of IgG, low affinity IIa, receptor for (CD32), Fc receptor, 20869 1256 M32062 N receptor, IgG, low affinity III) IgG, low affinity III) 1427 1209 L38644 N (Female sterile (2) Ketel, karyopherin (imporlin) belta 1) karyopherin (imporlin) beta 1 9452 373 AA955206 M (fibrinogen-like 2, fibrinogen-like protein 2) (fibrinogen-like 2, fibrinogen-like protein 2) 15295 164 AA875594 M,H,I (FK506 binding protein 1A, 12kDa, FK506-binding protein 2) FK506 binding protein 1A, 12kDa 6782 838 AI176170 B (FK506 binding protein 1A, 12kDa, FK506-binding protein 2) FK506 binding protein 1A, 12kDa 15296 907 AI228738 N,H,I (FK506 binding protein 1A, 12kDa, FK506-binding protein 2) FK506 binding protein 1A, 12kDa 15297 1118 D86641 N,K (FK506 binding protein 1A, 12kDa, FK506-binding protein 2) FK506 binding protein 1A, 12kDa (FK506 binding protein 4, FK506 binding protein 4, 59kDa, 13091 764 AI136977 L FK506-binding protein FKBP59) (FK506 bindig protein 4, FK506 binding protein 4, 59kDa) 16895 1313 M86240 N (fruclose bisphosphatase 1, fruclose-1,6-bisphosphatase 1) (fruclose bisphosphalase 1, fruclose-1,6-bisphosphalase 1) (Fruclose-bisphosphate aidolase class-I, aidoiase 1, a isoform, 7064 1220 M12919 N aidciase A, fructose-bisphosphale) (aidclase 1, A isoform, aidclase A, frucicsa-bisphosphale) (Fumarylacetoacelase, fumarylacetoacetase, fumarylacetoacetate hydrclase, fumarylacetoacetate hydrolase (fumarylacetoacetate hydrolase, fumarylacetoacetate hydrolase 23961 1298 M77694 M,N,E,G,I (fumarylacetoacetase)) (fumarylacetoacetase)) (G protein alphai subunit 65A, guanine nuclectide binding protein (guanine nucleotide binding protein (g protein), alpha inhibiting (G protein), alpha inhibilting activity polypeplide 2, guanine activity polypeplide 2, guanine nudectide binding protein, alpha 15887 154 AA875225 N nucleotide binding protein, alpha inhibiting 2) inhibiting 2) Table 3 GLGC GenBank Acc or Identifier Seq ID RefSeq ID Model Code Human Homologous Gene Name Human Homologous Cluster Tile (G protein alphai subunit 65A, guanine nucleotide binding protein (guanine nucleotide binding protein (G protein), alpha inhibiting (G protein), alpha inhibiting activity polypeptide 2, guanine activity polypeptide 2, guanine nucleotide binding protein, alpha 15888 154 AA875225 N nucleotide binding protein, alpha inhibiting 2) inhibiting 2) (G protein-coupled receptor, family C, group 2, member A, (G protein-coupled receptor, family C, group 2, member A, calcium- calcium-sensing receptor (hypocalciuric hypercalcernia 1, severe sensing receptor (hypocalciuric hypercalcemia 1, severe neonatal 45 1417 U10354 M,J,L neonatal hyperparathyroidism)) hyperparathyroidism)) (gamma-aminobutyrici acid (GABA-A) transporter 3, solule carrier (gamma-aminobutyric acid (GABA-A) transporter 3, solute carrier 729 1328 M95672 N,D family 6 (neurotransmitter transporter, GABA), member 13) family 6 (neurotransmitter transporter, GABA), member 13) 15072 1357 NM_144730 A (GATA binding protein 4, GATA-binding protein 4) GATA binding protein 4 (Glucose transporter 1, solute carrier family 2 (facililated glucose 16248 1376 S68135 N transporter), member 1, sugar transporter) solule carrier family 2 (facilitated glucose transporter), member 1 (glucose-6-phsophatase, catalytic, glucose-6-pphosphatase, (glucose-6-phosphatase, catalytic, glucose-6-phosphatase, catalytic 1321 1206 L37333 N catalytic (glycogen storage disease type I, von Gierke disease)) (glycogen storage disease type I, von Gierke disease)) (glucose-6-phosphatase, transport (glucose-6-phosphate) (glucose-t6-phosphatase, transport (glucose-6-phosphate) protein 1, 5496 507 AF080468 M,N,D,E protein 1, glucose-6-phosphatase, transport protein 1) glucose-6-phosphatase, transport protein 1) (glucose-6-phosphatase, transport (glucose-6-phosphate) (glucose-6-phsophatase, transport (glucose-6-phosphate) protein 1, 5497 507 AF080468 M,N,D,E protein 1, glucose-6-phosphatase, transport protein 1) glucose-6-phosphatase, transport protein 1) (Glutamate dehydrogenase, glutamate dehydrogenase, 4574 968 Al233216 N glutamate dehydrogenase 1) (glutamate dehydrogenase, glutamate dehydrogenase 1) (glutamate-cysteine ligase, modifier subunit, glutamate-cysteine (glutamate-cysteine ligase, modifier subunit, glutamate-cysteine 14003 1374 S65555 N,B,J ligase, modifier subunit) ligase, modifier subunit) (Glutamate-cysteine ligase catalytic subunit, glutamate-cysteine 1247 1163 J05181 N,J ligase, glutamate-cysteine-ligase, catalytic subunit) glutamate-cysteine ligase, catalytic subunit 1853 1511 X12367 N (glutathione peroxidase 1, similar to glutathione peroxidase 1) 4615 1061 D00680 N (glutathione peroxidase 3, glutathione peroxidase 3 (plasma)) (glutathione peroxidase 3, glutathione peroxidase 3 (plasma)) (glutathione S-transferase A5, glutathione S-transferase, alpha 2 (gluthione S-transferase A5, glutathione S-transferase, alpha 2 18989 1168 K00136 N (Yc2)) (Yc2)) 20817 582 Al012589 M,N (glutathione S-transferase pi, glutathione S-transferase, pi 2) (glutathione S-transferase pi, glutathione S-transferase, pi 2) 20818 1498 X02904 M,N (glutathione S-transferase pi, glutathione S-transferase, pi 2) (glutathione S-transferase pi, glutathione S-transferase, pi 2) (glycolate oxidase, hydroxyacid oxidase (glycolate oxidase) 3, (hydroxyacid oxidase (glycolate oxidase) 3, hydroxyacid oxidase 2 573 949 Al232087 N,J hydroxyacid oxidase 2 (long chain)) (long chain)) Table 3 GLGC GenBank Acc or Identifier Seq ID RefSeq ID Model Code Human Homologous Gene Name Human homologous Clusler Title (glycoprolein 38, lung type-I cell membrane-associaled 22675 1493 U92081 N,G glycoprolein) (glycoprolein 38, lung toye-1 cell membrane-associaled glycoprolein) (group specific component, group-specific component (vilamin D (group specific component, group-specific component (vilamin D 4254 1219 M12450 N tinding prolein)) binding prolein)) (growth arrest and DNA-damage-induclible 45 alpha, growth (growth arrest and DNA-damage-inducible 45 alpha, growth arrest 352 661 A1070295 H arrest and DNA-damage-induclible, alpha) and DNA-damage-incucible, alpha) (growth arrest and DNA-damage-inducible 45 alpha, growth (growth arrest and DNA-damage-inducible 45 alpha, growth arrest 353 1203 L32591 M,H,I arrest and DNA-damage-inducible, alpha) and DNA-damage-inducible, alpha) 9growth arrest and DNA-damage-inducible 45 alpha, growth (growth arrest and DNA-damage-inducible 45 alpha, growth arrest 354 1203 L32591 M,H,I arrest and DNA-damage-inducible, alpha) and DNA-damage-inducible, alpha) 25290 1102 D42148 N,J (growth arrest specific 6, growth arrest-specific 6) (growth arrest specific 6, growth arrest-specific 6) (Guanyl cyclase alpha-subunit at 99B, guanylale cyclase 1, 888 81 AA849036 N,B soluble, alpha 3) guanylate cyclase 1, soluble, alpha 3 (guanylate cyclase activator 1B (retina), guanylate cyclase (guanylate cyclase activator 1B (retina), guanylate cyclase activator activator 2 (guanylin 2, intestinal, healstable), guanylate cyclase 2 (guanylin 2, inteslinat, healstable), guanylate cyclase activator 2A 1976 1326 M95493 N activator 2A (guanylin)) (guanylin)) (H2A histone family, member Z, Histone H2A variant, histone 17661 1267 M37584 N,E H2A variant) H2A histone family, member Z 15642 861 AI177503 M,F,J (H3 histone, family 3B, H3 histone, family 3B (H3,3B)) (H3 histone, family 3B, H3histone, family 3B (H3,3B)) 20167 1523 X15705 E (heat shock 70kDa protein 2, heat shock protein 2) (heat shock 70kDa protein 2, heat shock protein 2) (heat shock 70kDa protein 8, heat shock cognate 71-kd protein, 17764 985 AI234604 N heat shock protein 1, heat shock prolein 8) (heat shock 70kDa protein 8, heat shock protein 8) (heat shock 70kDa protein 8, heat shock cognate 71-kd protein, 17765 1216 M11942 N heat shock protein 1, heat shock protein 8) (heat shock 70kDa protein 8, heat shock protein 8) 16518 845 AI176546 N,C,K (heat shock 90kDa protein 1, alpha, heat shock protein 1, alpha) (heat shock 90kDa protein 1, alpha, heat shock protein 1, alpha) 20795 1360 NM_175761 N,H (heat shock 90kDa protein 1, alpha, heat shock protein 1, alpha) (heat shock 90kDa protein 1, alpha, heat shock protein 1, alpha) (heat shock protein 47, serine (or cysteine) proteinase inhibitor, clade H (heat shock protein 47), member 1, (collagen binding (seine (or cysteine) proteinase inhibitor, clade H (heat shock protein protein 1), serine (or cysteine) proteinase inhibitor, clade H, 47), member 1, (collagen binding protein 1), serine (or cysteine) 17301 1292 M69246 N,E,I member 1) proteinase inhibitor, clade H, member 1) Table 3 GLGC GenBank Acc or Identifier Seq ID RefSeq ID Model Code Human Homologous Gene Name Human Homologous Cluster Title (Heat shock protein cognate 3, heat shock 70kD protein 5 (glucose-regulated protein), heat shock 70kDa protein 5 (glucose (heat shock 70kD protein 5 (glucose-regulated protein), heat shock 1466 1222 M14050 N regulated protein, 78kDa), heat shock protein) 70kDa protein 5 (glucose-regulated protein, 78kDa)) (hedgehog, sonic hedgehog, sonic hedgehog homolog 605 1199 L27340 C (Drosophila)) (sonic hedgehog, sonic hedgehog homolog (Drosophila)) (hemoglobin alpha, adult chain 1, hemoglobin alpha, adult chain (hemoglobin alpha, adult chain 1, hemoglobin, alpha 1, hemoglobin, 1685 97 AA851497 J 2, hemoglobin, alpha 1, hemoglobin, alpha 2) alpha 2) (hemoglobin alpha, adult chain 1, hemoglobin alpha, adult chain (hemoglobin alpha, adult chain 1, hemoglobin, alpha 1, hemoglobin, 1687 890 AI179971 J 2, hemoglobin, alpha 1, hemoglobin, alpha 2) alpha 2) (hemoglobin alpha, adult chain 1, hemoglobin alpha, adult chain (hemoglobin alpha, adult chain 1, hemoglobin, alpha 1, hemoglobin, 1688 932 AI230970 J 2, hemoglobin, alpha 1, hemoglobin, alpha 2) alpha 2) (hemoglobin alpha, adult chain 1, hemoglobin alpha, adult chain (hemoglobin alpha, adult chain 1, hemoglobin, alpha 1, hemoglobin, 1689 1009 AI236360 J 2, hemoglobin, alpha 1, hemoglobin, alpha 2) alpha 2) (hemoglobin alpha, adult chain 1, hemoglobin alpha, adult chain (hemoglobin alpha, adult chain 1, hemoglobin, alpha 1, hemoglobin, 1684 1547 X56325 J 2, hemoglobin, alpha 1, hemoglobin, alpha 2) alpha 2) (Henna, phenylalanine hydroxylase, phenylalanine-4- 6055 1218 M12337 M,N,D hydroxylase (PH4H)) phenylalanine hydroxylase (Hepatocyte nuclear factor 4, hepatic nuclear factor 4, 10860 1549 X57133 N hepatocyte nuclear fctor 4, alpha) (hepatic nuclear factor 4, hepatocyte nuclear factor 4, alpha) (Hepatocyte nuclear factor 4, hepatic nuclear factor 4, 25699 1549 X57133 N hepatocyte nuclear factor 4, alpha) (hepatic nuclear factor 4, hepatocyte nuclear factor 4, alpha) (Heterogeneous nuclear ribonucleoprotein at 98DE, 17502 1217 M12156 N heterogeneous nuclear ribonucleoprotein A1) heterogeneous nuclear ribonucleoprotein A1 (heterogeneous nuclear ribonucleoprotein D, heterogeneous (heterogeneous nuclear ribonucleoprotein D, heterogeneous nuclear nuclear ribonucleoprotein D (AU-rich element RNA binding ribonucleoprotein D (AU-rich element RNA binding protein 1, 25682 1530 X16933 N protein 1, 37kDa)) 37kDa)) (heterogeneous nuclear ribonucleoprotein U, heterogeneous (heterogeneous nuclear ribonucleoprotein U, heterogeneous nuclear 19834 1080 D14048 E nuclear ribonucleoprotein U (scaffold attachment factor A)) ribonucleoprotein U (scaffold attachment factor A)) 19110 1289 M64986 A,J (high-mobility group box 1, similar to Amphoterin) high-mobility group box 1 (hippocalcin-like 1, similar to neural visinin-like Ca2+-binding 24428 1074 D13126 N protein type 3) hippocalein-like 1 17345 202 AA892014 E (HLA-B associated transcript 1, HLA-B-associated transcript 1A) (HLA-B associated transcript 1, HLA-B associated transcript 1A) Table 3 GLGC GenBank Acc or Identifier Seq ID RefSeq ID Model Code Human Homologous Gene Name Human Homologous cluster Title (hm:zehn0976, tyrosine 3-monooxygenase/tryplophan 5- tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation 25279 1092 D30740 C monooxygenase activation protein, zeta polypeptide) protein, zeta polypeptide 14929 802 AI170353 M,G,K(hm:zehp0199, ribosomal protein L21) ribosomal protein L21 (HMT1 hnRNP methyltransferase-liek 2 (S. cerevisiae), (HMT1 hnRNP methyltransferase-like 2 (S. cerevisiae), heterogeneous nuclear ribonucleoproteins methyltransferase- heterogeneous nuclear ribonucleoproteins methyltransferase-like 2 20772 1470 U60882 N like 2 (S. cerevisiae)) (S. cerevisiae)) (hormone sensitive lipase, lipase, hormone sensitive, lipase, 783 1011 AI236589 F hormone-sensitive) (lipase, hormone sensitive, lipase, hormone-sensitive) (Hsp70/Hsp90 organizing protein homolog, stress-induced phosphoprotein 1, stress-induced-phosphoprotein 1 (stress-induced phosphoprotein 1, stress-induced-phosphoprotein 1 11840 1604 Y15068 H,I (Hsp70/Hsp90-organizing protein)) (Hsp70/Hsp90-organizing protein)) 23045 480 AF034218 N (hyaluronidase 1, hyaluronoglucosaminidase 1) (hyaluronidase 1, hyaluronoglucosaminidase 1) (hydroxyacyl-Coenzyme A dehydrogenase type II, hydroxyacyl- (hydroxyacyl-Coenzyme A dehydrogenase type II, hydroxyacyl- 15175 355 AA945583 E Coenzyme A dehydrogenase type II, scully) Coenzyme A dehydrogenase, type II) (hydroxysteroid (11-beta) dehydrogenase 2, hydroxysteroid 11- (hydroxysteroid (11-beta) dehydrogenase 2, hydroxysterold 11-beta 275 1434 U22424 M beta dehydrogenase 2) dehydrogenase 2) (hypothetical gene supported by AK036061, ribosomal protein 18612 904 AI228624 G L29) ribosomal protein L29 (hypothetical gene supported by X73829; AK011058; AK012665; AK019223; AK088660; BC027217; NM_009098, mg:ab03d05, 16204 1505 X06423 M,N,G ribosomal protein S8) ribosomal protein S8 (hypothetical gene supported by X73829; AK011058; AK012665; AK019223; AK088660; BC027217; NM_009098, mg:ab03d05, 16205 1505 X06423 N,F ribosomal protein S8) ribosomal protein S8 (hypothetical protein LOC123876, hypothetical protein 4589 498 AF062389 M,N,D MGC37245) (hypothetical protein LOC123876, hypothetical protein MGC 37245) (hypothetical protein LOC228785, myosin light chain kinase 2, (hypothetical protein LOC228785, myosin light chain kinase 2, 24459 1154 J03886 C skeletal muscle) skeletal muscle) (hypothetical protein LOC284889, macrophage migration (hypothetical protein LOC284889, macrophage migration inhibitory 15138 543 AI009801 C inhibitory factor) factor) (hypothetical protein LOC284889, macrophage migration (hypothetical protein LOC284889, macrophage migration inhibitory 15137 1385 S73424 L inhibitory factor) factor) Table 3 GLGC GenBank Acc or Identifier Seq ID RefSeq ID Model Code Human Homologous Gene Name Human Homologous Cluster Title (hypothetical protein MGC6357, lamina-associated polypeptide 1949 1431 U19614 A 1B) (hypothetical protein MGC6357, lamina-associated polypeplide 1B) 9952 170 AA891422 N (hypoxia induced gene 1, similar to HSPC010) (id:ibd5097, transforming growth factor beta 1 induced transcript (transforming growth factor beta 1 induced transcript 4, transforming 17401 1196 L25785 M,B,G 4, transforming growth factor beta-stimulated protein TSC-22) growth factor beta-stimulated protein TSC-22) (inhibitor of DNA binding 1, inhibitor of DNA binding 1, dominant (inhibitor of DNA binding 1, inhibitor of DNA binding 1, dominant 10248 1193 L23148 n negative helix-loop-helix protein) negative helix-loop-helix protein) (Inositol 1,4,5,-tris-phosphate receptor, inositol 1,4,5- triphosphate receptor, inositol 1,4,5-triphosphate receptor, type 1, similar to inositol 1,4,5-triphosphate receptor 1; InsP3R type I; 10464 1165 J05510 M,I Purkinje cell protein 1; opisthotonus) inositol 1,4,5-triphosphate receptor, type 1 (insulin-like growth factor 1, insulin-like growth factor 1 (insulin-like growth factor 1, insulin-like growth factor 1 21053 1226 M15481 M (somatomedin C)) (somatomedin C)) (intercellular adhesion molecule, intercellular adhesion molecule (intercellular adhesion molecule, intercellular adhesion molecule 1 2554 1063 D00913 M,N 1 (CD54), human rhinovirus receptor) (CD54), human rhinovirus receptor) (intercellular adhesion molecule, intercellular adhesion molecule (intercellular adhesion molecule, intercellular adhesion molecule 1 2555 1063 D00913 M,C,I 1 (CD54), human rhinovirus receptor) (CD54), human rhinovirus receptor) (interferon induced transmembrane protein 2 (1-8D), similar to 21659 560 AI010584 D interferon-inducible protein 16) interferon induced transmembrane protein 2 (1-8D) 17516 847 AI176621 A,E,L (Iron regulatory protein 18, aconitase 1, aconitase 1, solubie) (aconitase 1, aconitase 1, soluble) 1729 1342 NM_019147 N,B (jagged 1, jagged 1 (Alagille syndrome), jagged3) (jagged 1, jagged 1 (Alagille syndrome)) 5384 166 AA891041 I (Jun-B oncogene, Jun-related antigen, jun B proto-oncogene) (Jun-B oncogene, jun B proto-oncogene) 20161 1543 X54686 M,C,I (Jun-B oncogene, Jun-related antigen, jun B proto-oncogene) (Jun-B oncogene, jun B proto-oncogene) 16726 1352 NM_031855 M,N,E,G,H,I (kethexokinase, ketohexokinase (fructokinase)) (ketohexokinase, ketohexokinase (fructokinase)) (KH domain containing, RNA binding, signal transduction KH domain containing, RNA binding, signal transduction associated 11421 55 AA818199 E associated 1, wu:fc56c11) 1 794 1476 U68168 M,I (kynureninase, kynureninase (L-kynurenine hydrolase)) kynureninase (L-kynurenine hydrolase) 17807 1270 M54926 M,G (lactate dehydrogenase A, tactate dehydrogenase A4) lactate dehydrogenase A (lactate dehydrogenase, malate dehydrogenase 1, NAD (malate dehydrogenase 1, NAD (soluble), malate dehydrogenase, 4723 515 AF093773 N (soluble), malate dehydrogenase, soluble) soluble) 20086 590 AI013260 M,H (Lamin, lamin A, lamin A/C) (lamin A, lamin A/C) 20085 1572 X66870 C (Lamin, lamin A, lamin A/C) (lamin A, lamin A/C) Table 3 GLGC GenBank Acc or Identifier Seq ID RefSeq ID Model Code Human Homologous Gene Name Human Homologous Cluster Title 16871 1428 U18314 N,E (lamina-associated protein 2, thymopoietin) thymopcietin (laminin, beta 1, laminin, beta 2 9laminin S), similar to laminin, 22434 1333 NM_012974 F beta 2) laminin, beta 2 (laminin S) (lectin, galactoside-binding, soluble, 3, binding protein, (lectin, galactoside-binding, soluble, 3 binding protein, peptidylprolyl 16444 502 AF065438 N peptidylprolyl isomerase C-associated protein) isomerase C-associated protein) (Leukocyle-anligen-related-like, protein tyrosine phosphatase, receptor type, S, protein-tyrosine phosphatase with fibronectin 14978 858 AI177386 F type III-like domains (DPTP and LAR like)) protein tyrosine phosphatase, receplor type, S (lipase A, lysosomal acid, cholesterol esterase (Wolman (lipase A, lysosomal acid, cholesterol esterase (Wolman disease), 10260 1393 S81497 N disease). lysosomal acid lipase 1) lysosomal acid lipase 1) (lipase A, lysosomal acid, cholesterol esterase (Wolman (lipase A, lysosomal acid, cholesterol esterase (Wolman disease), 25563 1393 s81497 N disease), lysosomal acid lipase 1) lysosomal acid lipase 1) 1809 372 AA946503 G,K (lipocalin 2, lipocalin 2 (oncogene 24p3)) (lipocalin 2, lipocalin 2 (oncogene 24p3)) (Lissencephaly-1, platelet-activating factor acetylhydrolase, (platelet-activaling factor acetylhydrolase, isoform 1b, beta1 subunit, isoform 1b, beta 1 subunit, platelet-activating factor platelet-activating factor acetylhydrolase, isoform lb, alpha subunit 20753 43 AA801441 M,N,C,I acetylhydrolase, isoform lb, alpha subunit 45kDa) 45kDa) (low density lipid receptor-riated protein, low density lipoprotein receptor-related protein 2, low density lipoprotein-related prolein (low density lipoprotein receptor-related protein 2, low density 15110 182 AA891764 M,I 2) lipoprotein-related protein 2) (low density lipid receptor-riated protein, low density lipoprotein receptor-related protein 2, low density lipoprotein-related protein (low density lipoprotein receptor-related protein 2, low density 15111 1205 L34049 M,I 2) lipoprotein-related protein 2) (low density lipid receptor-rlated protein, low density lipoprotein receptor-related protein 2, low density lipoprotein-related protein (low density lipoprotein receptor-related protein 2, low density 15112 1205 L34049 N,I 2) lipoprotein-related protein 2) 21653 1022 AI237535 M,C,K (LPS-induced TN factor, lipopolysaccharide-induced TNF factor) (LPS-induced TN factor, lipopolysaccharide-induced TNF factor) 21654 1460 U53184 M,I,L (LPS-induced TN factor, lipopolysaccharide-induced TNF factor) (LPS-induced TN factor, lipopolysaccharide-induced TNF factor) 12450 729 AI103955 C (LRP16 protein, RIKEN cDNA D930010J01 gene) (LRP16 protein, RIKEN cDNA D930010J01 gene) (MAD homolog 2 (Drosophila), MAD, mothers against (MAD homolog 2 (Drosophila), MAD, mothers against 15242 459 AB017912 D decapentaplegic homolog 2 (Drosophila)) decapentaplegic homolog 2 (Drosophila)) Table 3 GLGC GenBank Acc or Identifier Seq ID RefSeq ID Model Code Human Homologous Gene Name Human Homologous Cluster Title (MAD homolog 2 (Drosophile), MAD, mothers against (MAD homolog 2 (Drosophila), MAD, mothers against 15243 459 AB017912 N decapentaplegic homolog 2 (Drosophila)) decapentaplegic homolog 2 (Drosophila)) (malate dehydrogenase 2, NAD (milochondrial), malate (malate dehydrogenase 2, NAD (mitochondrial), malate 165 778 AI145329 F dehydrogenase, mitochondrial) dehydrogenase, milochondrial) 13563 979 AI233773 E (MAWD binding protein, RIKEN cDNA 0610038K03 gene) (MAWD binding protein, RIKEN cDNA 0610038K03 gene) (MAX interacting protein 1, Max interacting protein 1, max 18070 462 AF003008 M,N interacting protein) (MAX interacting protein 1, Max interacting protein 1) (MCM6 minichromosome maintenance deficient 6 (MIS5 homolog, S. pombe) (S. cerevisiae), Minichromosome (MCM6 minichromosome maintenance deficient 6 (MIS5 homolog, maintenance 6, minichromosome maintenance deficient 6 (MIS5 S. pombe) (S. cerevislae), minichromosome mainlenance deficient 6 16676 1033 AI639082 N,E homolog, S. pombe) (S. cerevisiae)) (MIS5 homolog, S. pombe) (S, cerevisiae)) (MCM6 minichromosome maintenace deficient 6 (MIS5 homolog, S. pombe) (S. cerevislae), Minichromosome (MCM6 minichromosome maintenance deficient 6 (MIS5 homolog, maintenance 6, minichromosome maintenace deficient 6 (MIS5 S. pombe (S. cerevisiae), minichromosome maintenace deficient 6 16674 1425 U17565 E homolog, S. pombe) (S. cerevisiae)) (MIS5 homolog, S. pombe) (S. cerevisiae)) (MCM6 minichromosome mainlenance deficient 6 (MIS5 homolog, S. pombe) (S. cerevisiae), Minichromosome (MCM6 minichromosome maintenace deficient 6 (MIS5 homolog, maintenance 6, minichromosome maintenance deficient 6 (MIS5 S. pombe) (S. cerevisiae), minichromosome maintenance deficient 6 16675 1425 u17565 N,E homolog, S. pombe) (S. cerevisiae)) (MIS5 homolog, S. pombe)(S. cerevisiae)) (membrane metallo endopeptidase, membrane metallo- (membrane metallo endopeptidase, membrane metallo- endopeptidase (neutral endopeptidase, enkephalinase, CALLA, endopeptidase (neutral endopeptidase, enkephalinase, CALLA, 16849 292AA894298 N CD10), neprilysin) CD10)) 5837 1363 S43408 M,N,F (meprin 1 alpha, meprin A, alpha (PABA peptide hydrolase)) (meprin 1 alpha, meprin A, alpha (PABA peptide hydrolase)) 5838 1363 S43408 M,F,G (meprin 1 alpha, meprin a, alpha (PABA peptide hydrolase)) (meprin 1 alpha, meprin A, alpha (PABA peptide hydrolase)) (Metallo-beta-lactamase superfamily, hydroxyacyl glutathione 1409 589 AI012802 M,A,C,E,F hydrolase) hydroxyacyl glutathione hydrolase 15190 705 AI102562 M,N (metallothionein 1, metallothionein 1K) (metallothionein 1, metallothionein 1K) 15189 1215 M11794 N,B (metallothionein 1, metallothionein 1K) (metallothionein 1, metallothionein 1K) (methionine aminopeptidase 2, methionyl aminopeptidase 2, 8984 1180 L10652 D uninitiated) (methionine aminopeptidase 2, methionyl aminopeptidase 2) Table 3 GLGC GenBank Acc or Identifier Seq ID RefSeq ID Model Code Human Homologous Gene Name Human Homologous Cluster Title (methylenetetrahydrofolate dehydrogenase (NADP+ dependent), (methylenetetrahydrofolate dehydrogenase (NADP+ dependent), methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthase, methylenetetrahydrofolate dehydrogenase (NADP+ synthase, methylenetetrahydrofolate dehydrogenase (NADP+ dependent), methenyltetrahydrofolate cyclohydrolase, dependent), methenyltetrahydrofolate cyclohydrolase, 1549 1166 J05519 G formyltetrahydrofolate synthetase, tetrahydrofolate synthase) formyltetrahydrofolate synthetase) (microtubule-associated protein 1 light chain 3, microtubule- (microtubule-associated protein 1 light chain 3, microtubule- 23606 1406 U05784 N associated protein 1 light chain 3 beta) associated protein 1 light chain 3 beta) (mitochrondrial 2-oxoglutarate/malate carrier protein, solute carrier family 25 (mitochondrial carrier ; oxoglutarate carrier), solute carrier family 25 (mitochondrial carrier ; oxoglutarate carrier), 23300 1488 U84727 N member 11, wu : fa07h09) member 11 (mitogen-activated protein kinase kinase kinase 1, similar to Mitogen-activated protein kinase kinase kinase 1 (MAPK/ERK 1453 1456 U48596 F, K kinase kinase 1) (MEK kinase 1) (MEKK 1)) mitogen-activated protein kinase kinase kinase 1 (mitogen-activated protein kinase kinase kinase 1, similar to Mitogen-activated protein kinase kinase kinase 1 (MAPK/ERK 1454 1456 U48596 M, K kinase kinase 1) (MEK kinase 1) (MEKK 1)) mitogen-activated protein kinase kinase kinase 1 (Monooxygenase, cinnabar, kynurenine 3-monooxygenase 17324 495 AF056031 M (kynurenine 3-hydroxylase)) kynurenine 3-monooxygenase (kynurenine 3-hydroxylase) 11454 1245 M24604 M (mutagen-sensitive 209, proliferating cell nuclear antigen) proliferating cell nuclear antigen 11455 1245 M24604 M (mutagen-sensitive 209, proliferating cell nuclear antigen) proliferating cell nuclear antigen 24437 1239 M22357 A (myelin associated glycoprotein, myelin-associated glycoprotein) (myelin associated glycoprotein, myelin-associated glycoprotein) (myeloid differentiation primary response gene 116, protein (myeloid differentiation primary response gene 116, protein 11483 470 AF020618 M, l phosphatase 1, regulatory (inhibitor) subunit 15A) phosphatase 1, regulatory (inhibitor) subunit 15A) (myeloid differentiation primary response gene 116, protein (myeloid differentiation primary response gene 116, protein 18043 470 AF020618 F phosphatase 1, regulatory (inhibitor) subunit 15A) phosphatase 1, regulatory (inhibitor) subunit 15A) (myosin heavy chain IX, myosin, heavy polypeptide 9, non- 1970 1446 U31463 N, K muscle, zipper) (myosin heavy chain IX, myosin, heavy polypeptide 9, non-muscle) (Myosin heavy chain, myosin, heavy polypeptide 7, cardiac 20483 1524 X15939 N muscle, beta) myosin, heavy polypeptide 7, cardiac muscle, beta sulphate co-transporter like, solute carrier family 13 solute carrier family 13 (sodium-dependent dicarboxylate 1104 497 AF058714 N (sodium-dependent dicarboxylate transporter), member 2) transporter), member 2 Table 3 GLGC GenBank Acc or Identifier Seq ID RefSeq ID Model Code Human Homologous Gene Name Human Homologous Cluster Title (Na+/sulphate co-transporter like, solute carrier family 13 solute carrier family 13 (sodium-dependent dicarboxylate 25707 158 X59677 N (sodium-dependent dicarboxylate transporter), member 2) transporter), member 2 (NADH dehydrogenase (ubiquinone) flavoprotein 3, 10kDa, (NADH dehydrogenase (ubiquinone) flavoprotein 3, 10kDa, RIKEN 21211 433 AB000098 C RIKEN cDNA 1500032D16 gene) cDNA 15000032D16 gene) 14638 765 AI137049 J (Nijmegen breakage syndrome 1 (nibrin), nibrin) (Nijmegen breakage syndrome 1 (nibrin), nibrin) (nuclear distribution gene C homolog (A. nidulans), nuclear (nuclear distribution gene C homolog (A. niduians), nuclear 570 1590 X82445 N distribution gene C homolog (Aspergillus)) distribution gene C homolog (Aspergillus)) 1597 468 AF014503 L (nuclear protein 1, p8 protein (candidate of metastasis 1)) (nuclear prolein 1, p8 protein (candidate of metastais 1)) 20035 422 AA997933 M,H (nucleolar protein 5, nucleolar protein NOP5/NOP58) (nucleolar protein 5, nucleolar protein NOP5/NOP58) 25198 504 AF069782 M,N,I,K (nucleolar protein 5, nucleolar protein NOP5/NOP58) (nucleolar protein 5, nucleolar protein NOP5/NOP58) 8829 1271 M55015 M,A,F,K (nucleolin, wu:fa12d03) nucleolin (nucleophosmin (nucleolar phosphoprotein B23, numatrin), (nucleophosmin (nucleolar phosphoprotein B23, numatrin), 17394 1156 J03969 M,N,L nucleophosmin 1) nucleophosmin 1) (nucleophosmin (nucleolar phosphoprotein B23, numatrin), (nucleophosmin (nucleolar phosphoprotein B23, numatrin), 17393 1159 J04943 M,N nucleophosmin 1) nucleophosmin 1) 1401 1494 U93692 J (nucleoporin, nucleoporin 88kDa) (nucleoporin, nucleoporin 88kDa) (Nucleosome assembly protein 1, nucleosome assembly protein 22927 127 AA859920 N,E 1-liek 1) nucleosome asembly protein 1-like 1 (Nucleosome assembly protein 1, nucleosome assembly protein 16006 499 AF062594 M 1-lie 1) nucleosome assembly protein 1-like 1 (Nucleosome assembly protein 1, nucleosome assembly protein 16007 499 AF062594 N,E 1-like 1) nucleosome assembly protein 1-like 1 (Nucleosome assembly protein 1, nucleosome assembly protein 7665 622 AI030668 E 1-like 1) nucleosome assembly protein 1-like 1 (omithine aminotransferase, omithine aminotransferase (gyrate (omithine aminotransferase, ornithine aminotransferase (gyrate 4242 276 AA893325 N alrophy), omithine aminotransferse precursor) atrophy)) (omithine aminotransferase, omithine aminotransferase (gyrate (omithine aminotransferase, omithine aminotransferase (gyrate 25467 1321 M93297 N,G atrophy), omithine aminotransferse precursor) atrophy)) (Omithine decarboxylase 1, omithine decarboxylase, omithine 23523 1509 X07944 N decarboxylase 1, similar to Omithine decarboxylase (ODC) omithine decarboxylase 1 (PAI-1 mRNA-binding protein, similar to PAI-1 mRNA-binding (PAI-1 mRNA-binding protein, similar to PAI-1 mRNA-binding protein; chromodomain helicase DNA binding protein 3 protein; chromodomain helicase DNA binding protein 3 interacting 25589 1432 U21718 F interacting protein) protein) Table 3 GLGC GenBank Acc or Identifier Seq ID RefSeq ID Model Code Human Homologous Gene Name Human Homologous Cluster Title (Peptidyl-prolyl cis-trans isomerases, peptidylprolyl isomerase A, (peptidylprolyl isomerase A, peptidylprolyl isomerase A (cyclophilin 4392 906 A H peptidylprolyl isomerase A (cyclophilin A)) A)) 19252 204 AA892041 H (Peroxiredoxin 6005, peroxiredoxin 6) peroxiredoxin 6 19254 467 AF014009 H (Peroxiredoxin 6005, peroxiredoxin 6) peroxiredoxin 6 (peroxisomal biogenesis factor 11A, peroxisomal biogenesis (peroxisomal biogenesis factor 11A, peroxisomal biogenesis factor 4290 1058 AJ224120 L factor 11a) 11a) (peroxisomal membrane protein 2, peroxisomal membrane (peroxisomal membrane protein 2, peroxisomal membrane protein 405 1575 X70223 M, H, K protein 2, 22kDa) 2, 22kDa) (Phorbol esters/diacylglycerol binding domain (2 domains), Protein kinase C terminal domain, Protein C kinase 98E, protein 21029 24 M799981 C kinase C, eta) protein kinase C, eta (phosphate permease, solute carrier family 20 (phosphate transporter), member 1, solute carrier family 20, member 1, (solute carrier family 20 (phosphate transporter), member 1, solute 23538 708 AI102727 M wu : fa05g12) carrierfamily 20, member 1) 1340 1437 U25651 B (Phosphofructokinase, phosphofructokinase, muscle) phosphofructokinase, muscle (Phosphoglycerate kinase, phosphoglycerate kinase, phosphoglycerate kinase 1, similar to phosphoglycerate kinase 1312 1255 M31788 J 1) phosphoglycerate kinase 1 (phospholipase A2, group VI, phospholipase A2, group VI (phospholipase A2, group VI, phospholipase A2, group VI (cytosolic, 16147 1459 U51898 M, N (cytosolic, calcium-independent)) calcium-independent)) (phospholipase C, beta 1, phospholipase C, beta 1 (phospholipase C, beta 1, phospholipase C, beta 1 20414 1188 L14323 M (phosphoinositide-specific)) (phosphoinositide-specific)) (phospholipase D1, phospholipase D1, phophatidylcholine- 1535 437 AB000778 F specific) phospholipase D1, phospholipase D1, phophatidylcholine-specific) 13369 1087 D21132 (phosphotidylinositol transfer protein, beta, vibrator) phosphotidylinositol transfer protein, beta (pectin 1, intermediate filament binding protein 500kDa, short 1141 1557 X59601 M, C, G stop) plectin 1, intermediate filament binding protein 500kDa (pole hole, raf-related oncogene, v-raf murine sarcoma 3611 viral (raf-related oncogene, v-raf murine sarcoma 3611 viral oncogene 6577 1506 X06942 F oncogene homolog 1) homolog 1) 1798 354 AA945569 M, D (pregnancy zone protein, similar to alpha-2-macroglobulin) (propionyl Coenzyme A carboxylase, alpha polypeptide, (propionyl Coenzyme A carboxylase, alpha polypeptide, propionyl- 20481 1240 M22631 M, N, G, K propionyl-Coenzyme A carboxylase, alpha polypeptide) Coenzyme A carboxylase, alpha polypeptide) Table 3 GLGC GenBank Acc or Identifier Seq ID RefSeq ID Model Code Human Homologous Gene Name Human Homologous Cluster Title (prostatic binding protein, similar to hippocampal cholinergic 15599 1580 X75253 J neurostimulating peptide precursor protein) prostatic binding protein (proteasome (prosome, macropain) 28 subunit, beta, proteasome (prosome, macropain) activator subunit 2 (PA28 (proteasome (prosome, mcropain) 28 subunit, beta, proteasome 18751 93 AA851169 G beta), proteasome activator subunit 2) (prosome, macropain) activator subunit 2 (PA28 beta)) (proteasome (prosome, macropain) 28 subunit, beta, proteasome (prosome, macropain) activator subunit 2 (PA28 (proteasome (prosome, macropain) 28 subunit, beta, proteasome 18750 1105 D45250 N,G beta), proteasome activator subunit 2) (prosome, macropain) activator subunit 2 (PA28 beta)) (proteasome (prosome, macropain) subunit, alpha type 3, (proteasome (prosome, macropain) subunit, alpha type 3, 3987 1122 D90258 M,N proteasome (prosome, macropain) subunit, alpha type, 3) proteasome (prosome, macropain) subunit, alpha type, 3) (proteasome (prosome, macropain0 subunit, alpha type 6, proteasome (prosome, macropain) subunit, alpha type, 6, (proteasome (prosome, macropain) subunit, alpha type 6, 15538 758 AI112633 L proteasome (prosome, macropain) subunit, alpha type, 6a) proteasome (prosome, macropain) subunit, alpha type 6) (proteasome (prosome, macropain) subunit, alpha type 6, proteasome (prosome, macropain) subunit, alpha type, 6 (proteasome (prosome, macropain) subunit, alpha type 6, 15535 1069 D10755 L proteasome (prosome, macropain) subunit, alpha type, 6a) proteasome (prosome, macropain) subunit, alpha type, 6) (proteasome (prosome, macropain) subunit, beta tyep 6, (proteasome (prosome, macropain) subunit, beta type 6, 25253 1068 D10754 H proteasome (prosome, macropain) subunit beta type, 6) proteasome (prosome, macropain) subunit, beta type, 6) (Proteasome 29kD subunit, endopeptidase, proteasome (prosome, macropain) subunit, alpha type 4, proteasome (proteasome (prosome, macropain) subunit, alpha, tyep 4, 1447 1545 X55986 D (prosome, macropain) subunit, alpha type, 4) probeasome (prosome, macropain) subunit, alpha type, 4) (Proteasome alpha subunit, proteasome (prosome, macropain) subunit, alpha type 5, proteasome (prosome, macropain) (proteasome (prosome, macropain) subunit, alpha type 5, 3254 1070 D10756 N,L subunit, alpha type 5) proteasome (prosome, macropain) subunit, alpha type, 5) (protein C, protein C (inactivator of coagulation factors Va and (protein C, protein C (inactivator of coagulation factors Va and 556 1569 X64336 M,N Villa)) Villa)) 25405 1230 M18330 N (protein kinase, protein kinase C, delta) protein kinase C, delta (protein phosphatase 2 (formerly 2A), calalytic subunit, alpha (protein phosphalase 2 (formerly 2A), catalytic subunit, alpha 3202 1527 X16043 N isoform, protein phosphatase 2a, catalytic subunit, alpha isoform) isoform, protein phosphatase 2a, catalytic subunit, alpha isoform) (Protein tyrosine phosphatase 10D, protein tyrosine 245 1107 D45412 J phsophatase, receptor type, O) protein tyrosine phosphatase, receptor tyep, O Table 3 GLGC GenBank Acc or Identifier Seq ID RefSeq ID Model Code Human Homologous Gene Name Human Homologous Cluster Title (Protein lyrosine phosphatase 10D, protein tyrosine 247 1443 U28938 J phosphatase, receptor type, O) protein tyrosine phosphatase, receptor type, O (protein tyrosine phosphatase 4a1, protein tyrosine phosphatase (protein tyrosine phosphatase 4a1, protein tyrosine phosphatase 24219 1200 L27843 M,L type IVA, member 1, protein-tyrosine phosphotase) type IVA, member 1) (Protein tyrosine phosphatase 61F, hypothetical gene supported by AK085713, protein tyrosine phosphatase 1b, protein tyrosine 1844 1261 M33962 J phosphatase, non-receptor type 1) protein tyrosine phosphatase, non-receptor type 1 (pulative pyruvate dehydrogenase phosphatase isoenzyme 2, pyruvate dehydrogenase phosphatase isoenzyme 2, similar to [Pyruvate dehydrogenase [Lipoamidel]-phosphatase 2, mitochondrial precursor (PDP 2) (Pyruvate dehydrogenase 15761 500 AF062741 B phosphatase, catalytic subunit 2) (PDPC 2)) pyruvate dehydrogenase phosphatase isoenzyme 2 (pyridine nucleotide-disulphide oxidoreductase, thioredoxin 24235 169 AA891286 M,N,H,I reduclase 1) thicredoxin reductase 1 (pyridine nucleotide-disulphide oxidoreduclase, thioredoxin 23234 1474 U63923 M,A,I reductase 1) thioredoxin reductase 1 (Pyruvate dehydrogenase kinase, pyruvate dehydrogenase 1928 1418 U10357 N kinase, isoenzyme 2) pyruvate dehydrogenase kinase, isoenzyme 2 (Pyruvate dehydrogenase kinase, pyruvate dehydrogenase 1929 1418 U10357 N,A,C,D,E kinase, isoenzyme 2) pyruvate dehydrogenase kinase, isoenzyme 2 (Pyruvate kinase, pyruvate kinase liver and red blood cell, (pyruvate kinase liver and red blood cell, pyruvate kinase, liver and 20513 1503 X05684 N pyruvate kinase, liver and RBC) RBC) (RAB11A, member RAS oncogene family, RAB11a, member (RAB11A, member RAS oncogene family, RAB11a, member RAS 240 1297 M75153 N RAS oncogene family) oncogene family) 24651 1306 M83678 N (RAB13, member RAS oncogene family, hm:zeh0455) RAB13, member RAS oncogene family (RAB14, member RAS oncogene family, RAS-related protein, 20831 1307 M83680 B Rab-protein 14) RAB14, member RAS oncogene family (ras homolog gene family, member AB, ras homolog gene family, (ras homolog gene family, member AB, ras homolog gene family, 9541 300 AA900505 N,L member B) member B) 28 1093 D31662 M,F,G,I,J,L (regucalcin, regucalcin (senescence marker protein-30)) (regucalcin, regucalcin (senescence marker protein-30)) (regulator of G-protein signaling 19 interacting protein 1, (regulator of G-protein signaling 19 interacting protein 1, regulator of 15790 478 AF032120 E regulator of G-protein signaling 19 interacting protein 1) G-protein signaling 19 interacting protein 1) Table 3 GLGC GenBank Acc or Identifier Seq ID RefSeq ID Model Code Human Homologous Gene Name Human Homologous Cluster Title (regulator of G-protein signaling 19 interacting protein 1, (regulator of G-protein signaling 19 interacting protein 1, regulator of 15791 512 AF089817 C regulator of G-protein signaling 19 interacting protein 1) G-protein signaling 19 interacting protein 1) (retinol binding protein 1, cellular, similar to retinol binding protein 23806 1233 M19257 D 1, cellular) retinol binding protein 1, cellular (ribonuclease/angiogenin inhibitor, ribonuclease/angiogenin (ribonuclease/angiogenin inhibitor, ribonuclease/angiogenin inhibitor 18108 1566 X62528 N inhibitor 1) 1) (Ribose-phosphate pyrophosphokinase, phosphoribosyl 24582 1528 X16554 D pyrophosphate synthetase 1) phosphotribosyl pyrophosphate synthase 1 20812 356 AA945611 N (ribosomal protein 10, ribosomal protein L10) (ribosomal protein 10, ribosomal protein L10) 11849 1593 X93352 M,N,G (ribosomal protein L10A, ribosomal protein L10a) (ribosomal protein L10A, ribosomal protein L10a) 19112 1036 AI639157 J (Ribosomal protein L13 ribosomal protein L13) ribosomal protein L13 23854 1585 X78327 N,G (Ribosomal protein L13, ribosomal protein L13) ribosomal protein L13 19268 530 AI008641 D (Ribosomal protein L22, ribosomal protein L22) ribosomal protein L22 4259 207 AA892123 N (Ribosomal protein L36, ribosomal protein L36) ribosomal protein L36 15875 1563 X62145 N (Ribosomal protein L8, ribosomal protein L8) 25718 1563 X62145 M,G (Ribosomal protein L8, ribosomal protein L8) (Ribosomal protein P0, deoxyribonuclease, ribosomal protein, large, P0, similar to 60S acidic ribosomal protein P0 (L10E), 1069 1522 X15096 N similar to BLOCK 23) similar to BLOCK 23 24615 1318 M89646 N,D (ribosomal protein S24, similar to ribosomal protein S24) ribosomal protein S24 20839 177 AA891729 N (Ribosomal protein S27A, ribosomal protein S27a) ribosomal protein S27a 25686 1532 X51536 N,F (Ribosomal protein S3, ribosomal protein S3) 10109 1555 X58465 N,G (Ribosomal protein S5, ribosomal protein S5) 25702 1555 X58465 N,G (Ribosomal protein S5, ribosomal protein S5) (RIKEN cDNA 0610038C04 gene, secreted phosphoprotein 2, (RIKEN cDNA 0610038004 gene, secreted phosphoprotein 2, 18001 100 AA858573 M 24kDa) 24kDa) (RIKEN cDNA 0610038C04 gene, secreted phosphoprotein 2, (RIKEN cDNA 0610038C04 gene, secreted phosphoprotein 2, 17999 1430 U19485 M 24kDa) 24kDa) (RIKEN cDNA 0610038C04 gene, secreted phosphoprotein 2, (RIKEN cDNA 0610038C04 gene, secreted phosphoprotein 2, 18000 1430 U19485 I 24kDa) 24kDa) (RIKEN cDNA 1100001F19 gene, effele, ubiqutin-conjugating (RIKEN cDNA 1100001F19 gene, ubiqutin-conjugating enzyme E2D 15277 989 AI234889 D enzyme E2D 3 (UBC4/5 homolog, yeast)) 3 (UBC4/5 homolog, yeast)) Table 3 GLGC GenBank Acc or Idenlifier Seq ID RelSeq ID Model Code Human Homologous Gene Name Human Homologous Cluster Tile (RIKEN cDNA 1100001F19 gene, effete, ubiquitin-conjugating (RIKEN cDNA 1100001F19 gene, ubiquitin-conjugating enzyme E2C 15273 1421 U13177 E enzyme E2D 3 (UBC4/5 homolog, yeast)) 3 (UBC4/5 homolog. yeast)) (RIKEN cDNA 1300002P22 gene, enoyl-Coenzyme A. (RIKEN cDNA 1300002P22 gene, enoyl-Coenzyme A, hydratase/3- 17758 1173 K03249 N hydratase/3-hydroxyacyl Coenzyme A dehydrogenase) hydroxyacyl Coenzyme A dehydrogenase) (RIKEN cDNA 1500001M02 gene, death-associated prolein 6, myosin regulatory light chain 2, myosin regulatory light chain (RIKEN cDNA 1500001M02 gene, death-associaled protein 6, 20849 1502 X05566 M,G,K MRCL3, spaghetti squash) myosin regulatory light chain MRCL3) 8820 659 A1070152 B,H,L (RIKEN cDNA 1700037B15 gene, similar to Smhs1 protein) (RIKEN cDNA 1700037B15 gene, similar to Smhs1 protein) (RIKEN cDNA 2010004J23 gene, Ribosomal prolein L1. 1867 91 AA850940 N nbosomal prolein L1, ribosomal protein L4) (RIKEN cDNA 2010004J23 gene, ribosomal protein L4) 16847 1516 X13549 N (RIKEN cDNA 2210402A09 gene, ribosomal protein S10) (RIKEN cDNA 2210402A09 gene, ribosomal protein S10) 25606 1461 U53214 C (RIKEN cDNA 2410003M22 gene, tubulin-tyrosine ligase) (RIKEN cDNA 2410003M22 gene, tubulin-tyrosine ligase) (RIKEN cDNA 2410104119 gene, RNA-binding protein, fuse- (RIKEN cDNA 2410104119 gene, fuse-binding protein-interacting 10668 1010 AI236366 C binding protein-interacting repressor, poly U binding factor 68kD) repressor) (RIKEN cDNA 2810484M10 gene, hypothetical protein 2367 516 AF095741 N FLJ22390) (RIKEN cDNA 2810484M10 gene, hypothetical protein FLJ22390) (RIKEN cDNA 2810484M10 gene, hypothetical protein 2368 516 AF095741 N,K FLJ22390) (RIKEN cDNA 2810484M10 gene, hypothetical protein FLJ22390) (RIKEN cDNA 3010033P07 gene, Ribosomal protein S9, 16929 1571 X66370 G ribosomal protein S9) (RIKEN cDNA 3010033P07 gene, ribosomal protein S9) (RIKEN cDNA 3110039L19 gene, likely homolog of rat kinase D- (RIKEN cDNA 3110039L19 gene, likely homolog of rat kinase D- 6290 790 AI169232 C interacting substance of 220 kDa) interacting substance of 220 kDa0 (RIKEN cDNA 4930579A11 gene, likely ortholog of rat vacuole (RIKEN cDNA 4930579A11 gene, likely ortholog of rat vacuole 23166 129 AA859954 M,C,L membrane protein 1) membrane protein 1) 634 1170 K01932 N (RIKEN cDNA 5730496E24 gene, glutathione S-transferase A3) (RIKEN cDNA 5730496E24 gene, glutathione S-transferase A3) 25525 1383 S72505 N (RIKEN cDNA 5730496E24 gene, glutathione S-transferase A3) (RIKEN cDNA 5730496E24 gene, glutathione S-transferase A3) 635 1586 X78848 N (RIKEN cDNA 5730496E24 gene, glutathione S-transferase A3) (RIKEN cDNA 5730496E24 gene, glutathione S-transferase A3) Table 3 GLGC GenBank Acc or Identifier Seq ID RefSeq ID Model Code Human Homologous Gene Name Human Homologous Cluster Title (RIKEN cDNA 9030624013 gene, solute carrier lamily 9 (RIKEN cDNA 9030624O13 gene, solute carrier family 9 (sodium/hydrogen exchanger), isoform 3, solule carrier family 9 (sodium/hydrogen exchanger), isoform 3, solule carrier family 9 24496 1312 M85300 M,N,I,K (sodium/hydrogen exchanger), member 3) (sodium/hydrogen exchanger), member 3) (RIKEN cDNA A530050D06 gene, chromosome 14 open reading (RIKEN cDNA A530050D06 gene, chromosome 14 open reading 15703 444 AB009372 N frame 76) frame 76) (RIKEN cDNA D630043A20 gene, solute carrier family 22 (RIKEN cDNA D630043A20 gene, solute carrier family 22 (organic 15986 1602 Y09945 M,I (organic anion/cation transporter), member 9) anion/cation transporter), member 9) 19002 1043 AI639465 N (ring finger protein 28, ring finger protein 30) (ring finger protein 28, ring finger protein 30) 19003 1043 AI639465 F (ring finger protein 28, ring finger protein 30) (ring finger protein 28, ring finger protein 30) 21975 827 AI172247 N,B,L (rosy, xanthine dehydrogenase) xanthine dehydrogenase (RuvB-like 1 (E. coli), RuvB-like protein 1, Yeast hypothetical 1382 438 AB002406 G 50.5 KD protein like, pontin) (RuvB-like 1 (e. coli). RuvB-like prolein 1) (S100 calcium binding protein A10 (annexin II ligand, calpactin I, (S100 calcium binding prolein A10 (annexin II ligand, calpactin I, light polypeptide (p11)), S100 calcium binding protein A10 light polypeptide (p11)), S100 calcium binding protein A10 19040 1152 J03627 M,C,G,K (calpactin)) (calpactin)) (SAC1 (supressor of actin mulations 1, homolog)-like (S. cerevisiae), SAC1 suppressor of actin mutations 1-like (yeast), (SAC1 (supressor of actin mulations 1, homolog)-like (S. cerevisiae). 13618 929 AI230724 M,I Yeast recessive suppressor RSD1 like) SAC1 suppressor of actin mutations 1-like (yeast)) 13542 247 AA892798 N,B (sclerostin domain containing 1, sclerostin-like) (cystine-knot containing secreted protein, sclerostin-like) 2439 479 AF032668 A,F (SEC15 (S. cerevisiae)-like, SEC15 homolog (S. cerevisiae)) (SEC15 (S. cerevislae)-like, SEC15 homolog (S. cerevisiae)) (secreted phosphoprotein 1, secreted phosphoprotein 1 (osteopontin, bone sialoprotein I, early T-lymphocyte activation (secreted phosphoprotein 1, secreled phosphoprotein 1 23651 1223 M14656 M,G,K 1)) (osteopontin, bone sialoprotein I, early T-lymphocyle activation 1)) (sepiapterin reduclase, sepiapterin reductase (7,8- (seplaplerin reduclase, sepiaplerin reductase (7,8- 21400 1266 M36410 C,F dihydrobiopterin:NADP+ oxidoreduclase)) dihydrobiopterin:NADP+ oxidoreductase)) 9serine (or cysteine) proteinase inhibitor, clade E (nexin, (serine (or cysteine) proleinase inhibitor, clade E (nexin, plasminogen activalor inhibitor type 1), member 1, serine (or plasminogen activator inhibilor type 1), member 1, serine (or 15540 1243 M24067 K cysteine) proteinase inhibitor, clade E, member 1) cysteine) proteinase inhibitor, clade E, member 1) 3549 1181 L11319 N (signal peptidase complex, signal peptidase complex (18kD)) (signal peptidase complex, signal peptidase complex (18kD)) (signal sequence receptor, delta, signal sequence receptor, delts (signal sequence receptor, delta, signal sequence receptor, delta 9125 67 AA819338 n (translocon-associated protein delta)) (translocon-associated protein delta)) Ttable 3 GLGC GenBank Acc or Identifier Seq ID RefSeq ID Model Code Human Homologous Gene Name Human Homologous Cluster Title (signal transducer and activator of transcription 3, signal transducer and activator of transcription 3 (acute-phase response factor), signal transduction and activation of (signal transducer and activator of transcription 3, signal transducer 343 1592 X91810 L transcription 3) and activator of transcription 3 (acute-phase response factor)) 9silica-induced gene 41, splicing factor, arginine/serine-rich 10 (silica-induced gene 41, splicing factor, arginine/serine-rich 10 23307 99 AA851749 D (transformer 2 homolog, Drosophila)) (transformer 2 homolog, Drosophila)) (similar to KIAA1938 protein, solule carrier family 7 (cationic solute carrier family 7 (cationic amino acid transporter, y+ system), 24762 1362 NM_181092 M,D amino acid transporter, y+ system), member 8) member 8 9similar to ribosomal prolein S2, similar to ribosomal protein S2; 10267 1550 X57432 N 40S ribosomal protein S2) 6796 711 AI102753 M,B (similar to RING finger protein 4, similar to ring finger protein 4) similar to RING finger protein 4 (similar to solute carrier family 28 (sodium-coupled nuclecside transporter), member 1, solute carrier family 28 (sodium-coupled solule carrier family 28 (sodium-coupled nucleoside transporter), 714 1416 U10279 N nucleoside transporter), member 1) member 1 (similar to solute carrier family 7 (calionic amino acid transporter, y+ system), member 7, solute carrier family 7 (cationic amino solule carrier family 7 (cationic amino acid transporter, y+ system), 7300 786 AI169077 C acid transporter, y+ system), member 7) member 7 (similar to Tropomyosin alpha 4 chain 9Tropomyosin 4) 18528 924 AI230284 K (TM30p1), tropomyosin 4) tropomyosin 4 (similar to Tropomyosin alpha 4 chain (Tropomyosin 4) 18529 928 AI230716 M,K (TM30p1), tropomyosin 4) tropomyosin 4 (similar to Tropomyosin alpha 4 chain (Tropomyosin 4) 1514 1142 J02780 N (TM30p1), tropomyosin 4) tropomyosin 4 (sodium channel, nonvoltage-gated 1 alpha, sodium channel, (sodium channel, nonvoltage-gated 1 alpha, soldium channel, 24640 1576 X70521 N nonvoltage-gated, type 1, alpha polypeptide) nonvoltage-gated, type I, alpha polypeptide) (sodium channel, nonvoltage-gated 1 beta, sodium channel, (sodium channel, nonvoltage-gated 1 beta, sodium channel, 24639 1584 X77932 N nonvoltage-gated 1, beta (Liddle syndrome)) nonvoltage-gated 1, beta (Liddle syndrome)) (sodium channel, voltage gated, type VIII, alpha, sodium (sodium channel, voltage gated, type VIII, alpha, sodium channel, 117 490 AF049239 N channel, voltage-gated, type VIII, alpha polypeptide) voltage-gated, type VIII, alpha polypeptide) (solute carrier family 12 (sodium/chloride transporters), member (solule carrier family 12 9sodium/chloride transporters), member 3, 645 412 AA965132 G,K 3, solute carrier family 12, member 3) solute carrier family 12, member 3) (solute carrier family 12 (sodium/chloride transporters), member (solule carrier family 12 9sodium/chloride transporters), member 3, 646 1415 U10097 N,G,K 3, solute carrier family 12, member 3) solute carrier family 12, member 3) Table 3 GLGC GenBank Acc or Identifier Seq ID RefSeq ID Model Code Human Homologous Gene Name Human Homologous Cluster Title (solute carrier family 12 (sodium/potassium/chloride (solute carrier family 12 (sodium/potassium/chloride transporters), 4532 1414 U10096 J transporters), member 1, solute carrier family 12, member 1) member 1, solute carrier family 12, member 1) (solute carrier family 19 (foldate transporter), member 1, solute (solute carrier family 19 (folate transporter). member 1, solute carrier 23826 1451 U38180 N carrier family 19 9sodium/hydrogen exchanger), member 1) family 19 (sodium/hydrogen exchanger), member 1) 9solute carrier family 21 (organic anion transporter), member 1, (solute carrier family 21 (organic anion transporter), member 1, 24770 1191 L19031 M,N,G,I,J solulte carrier family 21 (organic anion transporter), member 3) solute carrier family 21 (organic anion transporter), member 3) (solute carrier family 3 (cystine, dibasic and neutral amino acid (solute carrier family 3 (cystine, dibasic and neutral amino acid transporters, activator of cystine, dibasic and neutral amino acid transporters, activator of cystine, dibasic and neutral amino acid 1622 1300 M80804 N transport), member 1, solute carrier family 3, member 1) transport), member 1, solute carrier family 3, member 1) (solute carrier family 34 (sodium phosphate), member 1, solute 18078 176 AA891726 N carrier family 34 (sodium phosphate), member 2) solute carrier family 34 (sodium phosphate), member 1 (solute carrier family 34 (sodium phosphate), member 1, solute 18075 454 AB013455 N carrier family 34 (sodium phosphate), member 2) solute carrier family 34 (sodium phosphate), member 1 (solute carrier family 34 (sodium phosphate), member 1, solute 18076 454 AB013455 N carrier family 34 (sodium phosphate), member 2) solute carrier family 34 (sodium phosphate), member 1 (solute carrier family 34 (sodium phosphate), member 1, solute 18077 740 AI105198 N carrier family 34 (sodium phosphate0, member 2) solute carrier family 34 (sodium phosphate), member 1 9solute carrier family 39 (iron-regulated transporter), member 1, 4956 1485 U76714 H solute carrier family 40 (iron-regulated transporter), member 1) solute carrier family 40 (iron-regulated transporter), member 1 (solute carrier family 39 (iron-regulated transporter), member 1, 4957 1485 U76714 N solute carrier family 40 (iron-regulated transporter), member 1) solute carrier family 40 (iron-regulated transporter), member 1 (solute carrier family 4 (anion exchanger), member 4, solute (solute carrier family 4 (anion exchanger), member 4, solute carrier 1511 463 AF004017 D carrier family 4, sodium bicarbonate cotransporter, member 4) family 4, sodium bicarbonate cotransporter, member 4) 1877 1579 X74593 A,D,E (Sorbitol dehydrogenase 1, sorbitol dehydrogenase) sorbiol dehydrogenase 20702 946 AI231821 N (stathmin 1, stathmin 1/oncoprotein 18) (stathmin 1, stathmin 1/oncoprotein 18) (Succinyl coenzyme A synthetase flavoprotein subunit, flavoprotein, succinate dehydrogenase complex, subunit A, 17514 324 AA925554 E,G flavoprotein (Fp)) succinate dehydrogenase complex subunit A, flavoprotein (Fp) (sulfotransferase family 1A, phenol-preferring, member 1, sulfotransferase family, cytosolic, 1A, phenol-preferring, member (solfotransferase family 1A, phenol-preferring, member 1, 4748 1192 l19998 N 1) sulfotransferase family, cytosolic, 1A, phenol-preferring, member 1) Table 3 GLGC GenBank Acc or identifier Seq ID RefSeq ID Model Code Human Homologous Gene Name Human Homologous Cluster Title (solfotransferase family 1A, phenol-preferring, member 1, sulfotransferase family, cytosolic, 1A, phenol-preferring, member (sulfotransferase family 1A, phenol-preferring, member 1, 4749 1192 L19998 N,L 1) sulfotransferase family, cytosolic, 1A, phenol-preferring, member 1) (Suppressor of profilin 2, actin related protein 2/3 complex, 9actin related protein 2/3 complex, subunit 1B, actin related protein 10015 509 AF083269 M,G,K subunit 1B, actin related protein 2/3 complex, subunit 1B, 41kDa) 2/3 complex subunit 1B 41kDa) (Suppressor of profilin 2, actin related protein 2/3 complex, (actin related protein 2/3 complex, subunit 1B, actin related protein 10016 509 AF083269 M,G subunit 1B, actin related protein 2/3 complex, subunit 1B, 41kDa) 2/3 complex, subunit 1B, 41kDa) (synaplosomal-associaled protein, synaptosomal-associated (synaplosomal-asociated protein, synaptosomal-associated 15800 481 AF035822 A protein 29kDa) protein, 29kDa) (syndecan 2, syndecan 2 (heparan sulfate protecglycan 1, cell (syndecan 2, syndecan 2 (heparan sulfate proleoglycan 1, cell 3995 566 AI011678 M,I,K surface-associated, fibroglycan)) surface-associated, fibroglycan)) (syndecan 2, syndecan 2 (heparan sulfate proteoglycan 1, cell (syndecan 2, syndecan 2 (heparan sulfate proteoglycan 1, cell 1529 1302 M81687 M,B,F,I surface-associated, fibroglycan)) surface-associated, fibroglycan)) 19768 222 AA892373 M,C,G (syndecan binding protein, syndecan binding protein (syntenin)) (syndecan binding protein, syndecan binding protein (syntenin)) (TCF3 (E2A) fusion partner. TCF3 (E2A) fusion pariner (in (TCF3 (E2A) fusion pariner, TCF3 (E2A) fusion pariner (in childhood 3407 423 AA997953 F childhood Leukemia)) Leukemia)) (testis enhanced gene transcript, testis enhanced gene transcript (testis enhanced gene transcript, testis enhanced gene transcript 24626 1581 X75856 N (BAX inhibitor 1)) (BAX inhibitor 1)) 18902 158 AA875390 N (thioredoxin-like, thioredoxin-like, 32kDa) (thioredoxin-like, thioredoxin-like, 32kDa) (thiosulfate sulfurtransferase (rhodanese), thiosulfate (thiosulfate sulfurtransferase (rhodanese), thiosulfate 21122 1546 X56228 N.E sulfurtransferase, mitochondrial) sulfurtransferase, milochondrial) (thiosulfate sulfurtransferase (rhodanese), thiosulfale (thiosulfate sulfurtranslerase (rhodanese), thiosulfate 21123 1546 X56228 N,D sulfurtransferase, mitochondrial) sulfurtransferase, mitochondrial) 19402 140 AA874848 N (Thy-1 co-transcribed, thymus cell antigen 1, theta) (Thy-1 co-transcribed, thymus cell antigen 1, theta) (thyroid hormone receptor alpha, thyroid hommone receptor. alpha (erythroblastic leukemia viral (v-erb-a) oncogene homolog. (thyroid hormone receptor alpha, thyroid hormone receptor, alpha 1814 1253 M31174 N avian)) (erythroblastic leukemia viral (v-erb-a) oncogene homolog, avian)) (Tis11 homolog, wu:fb80h11, zinc finger protein 36, C3H type- 20919 756 AI112516 N like 1) zinc finger protein 36, C3H type-like 1 Table 3 GLGC GenBank Acc or Identifier Seq ID RefSeq ID Model Code Human Homologous Gene Name Human Homologous Cluster Trtle (Tis11 homolog, wu:fb80h11, zinc finger protein 36, C3H type- 20920 763 AI136891 N like 1) zinc finger protein 36, C3H type-like 1 16039 9 AA799452 H (Transaldolase, transaldolase 1) transaldolase 1 7505 282 AA893702 N,A (transcobalamin 2, transcobalamin II; macrocytic anemia) (transcobalamin 2, transcobalamin II; macrocytic anemia) (transformation related protein 53, tumor protein p53 (Li- (transformation related protein 53, tumor protein p53 (Li-Fraumeni 17377 1514 X13058 N Fraumeni syndrome)) syndrome)) (Transketolase, branched chain keto acid dehydrogenase E1, (branched chain kelo acid dehydrogenase E1, alpha polypeptide alpha polypeptide (maple syrup urine disease), branched chain (maple syrup urine disease), branched chain ketoacid 17284 1145 J02827 N,G keloacid dehydrogenase E1, alpha polypeptide) dehydrogenase E1, alpha polypeptide) (Transketolase, branched chain keto acid dehydrogenase E1, (branched chain keto acid dehydrogenase E1, alpha polypeptide alpha polypeptide (maple syrup urine disease), branched chain (maple syrup urine disease), branched chain ketoacid 17285 1145 J02827 N ketoacid dehydrogenase E1, alpha polypeptide) dehydrogenase E1, alpha polypeptide) 20804 567 AI011684 H (transketolase, transketolase (Wernicke-Korsakoff syndrome)) (transketolase, transkelolase (Wernicke-Korsakoff syndrome)) 20802 655 AI059508 N,H (transketolase, transketolase (Wernicke-Korsakoff syndrome)) (transketolase, transketolase (Wernicke-Korsakoff syndrome)) 20803 1413 U09256 N,B,H,I (transketolase, transketolase (Wernicke-Korsakoff syndrome)) (transketolase, transketolase (Wernick-Korsakoff syndrome)) (transmembrane 4 superfamily member 11, transmembrane 4 (transmembrane 4 superfamily member 11, transmembrane 4 6641 1613 Z49858 M,A,I superfamily member 11 (plasmolipin)) superfamily member 11 (plasmolipin)) 24843 1301 M80826 N,J (trefoil factor 3 (intestinal), trefoil factor 3, intestinal) (lrefoil factor 3 (intestinal), trefoil factor 2, inlestinal) 15489 1458 U50194 F (Tripeptidyl-peptidase II, tripeptidyl peptidase II) tripeptidyl peplidase II 455 1225 M15474 N,E (Tropomyosin 1, tropomyosin 1 (alpha), tropomyosin 1, alpha) (tropomyosin 1 (alpha), tropomyosin 1, alpha) 457 1282 M60666 E,G,K (Tropomyosin 1, tropomyosin 1 (alpha), tropomyosin 1, alpha) (tropomyosin 1 (alpha), tropomyosin 1, alpha) 17161 219 AA892333 M (tubulin, alpha 1, tubulin, alpha 3) (tubulin, alpha 1, tubulin, alpha 3) 17160 792 AI169370 N (tubulin, alpha 1, tubulin, alpha 3) (tubulin, alpha 1, tubulin, alpha 3) 17159 1131 J00797 M,G,K (tubulin, alpha 1, tubulin, alpha 3) (tubulin, alpha 1, tubulin, alpha 3) 17158 1496 V01227 N (tubulin, alpha 1, tubulin, alpha 3) (tubulin, alpha 1, tubulin, alpha 3) (tumor necrosis factor receptor superfamily, member 12A, tumor (tumor necrosis factor receptor superfamily, member 12A, tumor 23314 393 AA957270 H,I necrosis factor receptor superfamily, member 12a) necrosis factor receptor superfamily, member 12a) 18647 1379 S69316 N (tumor rejection antigen (gp96) 1, tumor rejection antigen gp96) 15376 153 AA875206 N (ubiquilin 1, wu:fb48e11) ubiquilin 1 (Ubiquitin conjugating enzyme, ubiquitin conjugating-protein, ubiquitin-conjugating enzyme E2B (RAD6 homolog), ubiquitin- (ubiquitin-conjugating enzyme E2B (RAD6 homolog), ubiquitin- 17378 1284 M62388 N,D conjugating enzyme E2B, RAD6 homology (S. cerevisiae)) conjugating enzyme E2B, RAD6 homology (S. cerevisiae)) Table 3 GLGC GenBank Acc or Identifier Seq ID RefSeq ID Model Code Human Homologous Gene Name Human Homologous Cluster Title (UDP glycosyltransferase 1 family, polypeptide A cluster, UDP glycosyltransferase 1 family, polypeptide A6, similar to phenol 15126 1113 D83796 N UDP-glucuronosyltransferase) (UDP glycosyltransferase 1 family, polypeptide A cluster, UDP glycosyltransferase 1 family, polypeptide A6, similar to phenol 15124 1134 J02612 N,B UDP-glucuronosyltransferase) (UDP glycosyltransferase 1 family, polypeptide A clusler, UDP glycosyltransferase 1 family, polypeptide A6, similar to phenol 15125 1162 j05132 N,B UDP-glucuronosyltransferase) (UDP glycosyltransferase 1 family, polypeptide A cluster, UDP glycosyltransferase 1 family, polypeptide A6, similar to phenol 15127 1370 S56937 N UDP-glucuronosyltransferase) (UDP-GalbetaGlcNAc beta 1,4- galactosyltransferase, (UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, polypeptide polypeptide 6, UDP-Gal:betaGlcNAc beta 1,4- 6, UDP-Gal:betaGlcNAc beta 1,4-galactosyltransferase, polypeptide 10241 489 AF048687 N,C,K galaclosyltransferase, polypeptide 6) 6) (UDP-glucose dehydrogenase, UDP-glucose dehydrogenase, 18597 455 AB013732 N,B,H SQuashed Vulva, sugariess) UDP-glucose dehydrogenase (uromodulin, uromodulin (uromucoid, Tamm-Horsfall 16211 1386 S75960 N glycoprolein)) (urcmodulin, uromodulin (uromucoid, Tamm-Horsfall glycoprolein)) 9vacuolar protein sortin 4A (yeast), vacuolar protein sortin 4a (vacuolar protein sorting 4A (yeast), vacuolar protein sorting 4a 2979 289 AA894099 H (yeast), wu:fc57d08) (yeast)) 20443 1422 U14192 H (vesicle docking protein, vesicle docking protein p115) (vesicle docking prolein, vesicle docking protein p115) (viperin, viral hemorhagic septicemia wirus(VHSV) induced gene 4594 1599 Y07704 N 1) (viperin, viral hemorrhagic septicemia virus(VHSV) induced gene 1) (v-maf musculoaponeurotic fibrosarcoma (avian) oncogene homolog, v-maf musculoaponeurotic fibrosarcoma oncogene 989 1464 U56242 N,D,F homolog (avian)) v-maf musculoaponeurotic fibrosarcoma oncogene homolog (avian) (von Hippel-Lindau syndrome, von Hippel-Lindau syndrome (von Hippel-Lindau syndrome, von Hippel-Lindau syndrome 1424 1423 U14746 N homolog) homolog) 24900 1420 U12973 N,H (X transporter protein 2, hypothetical protein FLJ31236) (X transporter protein 2, similar to X transporter protein 2) (zinc finger protein 36, zinc finger prolein 36, C3H type, homolog (zinc finger protein 36, zinc finger protein 36, C3H type, homolog 13930 31 AA800613 M (mouse)) (mouse)) Table 3 GLGC GenBank Acc or Identifier Seq ID RefSeq ID Model Code Human Homologous Gene Name Human Homologous Cluster Title (Zinc finger, C2H2 type (3 domains), early growth response 1, 23868 474 AF023087 M,L stripe) early growth response 1 (Zinc finger, C2H2 type (3 domains), early growth response 1, 23872 1231 M18416 M stripe) early growth response 1 (Zinc finger, C2H2 type (3 domains), early growth response 1, 23869 1479 U75397 L stripe) early growth response 1 (Zwischenferment, glucose-6-phosphate dehydrogenase, glucose-6-phosphate dehydrogenase 2, glucose-6-phosphate-1 (glucose-6-phosphate dehydrogenase, glucose-6-phosphate 1399 1508 X07467 M,H,I dehydrogenase) dehydrogenase 2) 15408 1060 D00569 N 2,4-dienoyl CoA reductase 1, mitochondrial 2,4-dienoyl CoA reductase 1, milochondrial 15409 1060 D00569 N,L 2,4-dienoyl CoA reductase 1, mitochondrial 2,4-dienoyl CoA reductase 1, milochondrial 20493 1090 D28339 M,N 3-hydroxyanthranilate 3,4-dioxygenase 3-hydroxyanthranilate 3,4-dioxygenase 20494 1103 D44494 N,E 3-hydroxyanthraniliate 3,4-dioxygenase 3-hydroxyanthranilate 3,4-dioxygenase a disintegrin-like and metalioprotease (reprolysin type) with a disintegrin-like and metalloprolease (reprolysin type) with 22626 811 AI171159 M,K thrombospondin type 1 motif, 1 thrombospondin type 1 motif, 1 347 1400 U01914 D A kinase (PRKA) anchor prolein 8 A kinase (PRKA) anchor protein 8 24649 991 AI234950 C,K acid phosphatase 2, lysosomal acid phosphatase 2, lysosomal 24431 1285 M63282 M,F activating transcription factor 3 activating transcription factor 3 13104 552 Ai010224 D adducin 3 (gamma) adducin 3 (gamma) 16708 1465 U57042 M,N adenosine kinase adenosine kinase 16272 1582 X76456 N afamin afamin 820 225 AA892395 N aldolase B, fruclose-bisphosphate aldolase B, fructose-bisphosphate 818 1497 X02291 N aldolase B, fruclose-bisphosphate aldolase B, fructose-bisphosphate 15032 1490 U89905 M,A,H,I,K,L alpha-methylacyl-CoA racemase alpha-methylacyl-CoA racemase 18564 33 AA800745 M aminolevulinate, deite-, dehydratase aminolevulinate, delta-, dehydratase 7197 820 AI171962 M,G,K,L annexin A1 annexin A1 7196 1371 S57478 M,E,G,K annexin A1 annexin A1 574 1182 L13039 M,E,G,K annexin A2 annexin A2 16649 491 AF051895 M,N,E annexin A5 annexin A5 16650 1101 D42137 E annexin A5 annexin A5 1509 435 AB000507 N,A aquaporin 7 aquaporin 7 18727 1078 D13978 N argininosuccinate lyase argininosuccinate lyase Table 3 GLGC GenBank Acc or Identifier Seq ID RefSeq ID Model Code Human Homologous Gene Name Human Homologous Clusler Title 21339 409 AA964962 J,L ATP-binding cassette, sub-family A (ABC1), member 1 ATP-binding cassette, sub-family A (ABC1), member 1 15701 447 AB010467 A,I ATP-binding cassette, sub-family C (CFTR/MRP), member 3 ATP-binding cassette, sub-family C (CFTR/MRP), member 3 4361 1127 H31839 N BCL2-antagonist/killer 1 BCL2-antagonist/killer 1 439 1609 Z22607 N,F bone morphogenetic protein 4 bone morphogenetic protein 4 18246 1081 D14441 N,B,F brain abundant, membrane attached signal protein 1 brain abundant, membrane attached signal protein 1 24643 1477 U68417 N,K branched chain aminotransferase 2, mitochondrial branched chain aminotransferase 2, mitochondrial 16967 1337 NM_013146 E caldesmon 1 caldesomon 1 355 1375 S66D24 N cAMP responsive element modulator cAMP responsive element modulator 356 1375 S66024 N cAMP responsive element modulator cAMP responsive element modulator 20555 1439 U26033 F camitine O-octanoyltransferase camitine O-octanoyltransferase 9109 1269 M38135 N cathepsin H cathepsin H 1894 1176 L03201 N,B,L cathepsin S cathepsin S 21682 635 AI045030 N CCAAT/enhancer binding protein (C/EBP), della CCAAT/enhancer binding protein (C/EBP), delta 21683 1290 M65149 M,C,I.L CCAAT/enhancer binding protein (C/EBP), delta CCAAT/enhancer binding protein (C/EBP), delta 4412 26 AA800005 N CD151 antigen CD151 antigen 12903 1538 X53517 N CD37 antigen CD37 antigen 985 492 AF053312 N chemokine (C-C motif) ligand 20 chemokine (C-C molif) ligand 20 1306 1065 D10262 N cholin kinase choline kinase 24484 1454 U42976 H cholinergic receptor, nicotinic, beta polypeptide 4 cholinergic receptor, nicotinic, bela polypeptide 4 16350 1056 AJ011811 G claudin 7 claudin 7 16351 1056 AJ011811 G claudin 7 claudin 7 15259 870 AI178135 N complement component 1, q subcomponent binding protein complement component 1, q subcomponent binding protein 21443 1577 X71127 M,L complement component 1, q subcomponent, beta polypeptide complement component 1, q subcomponent, beta polypeptide 954 460 AF000114 B contacin associated protein 1 contacin associated protein 1 3454 477 AF030091 N,J cyclin L1 cyclin L1 15028 336 AA942685 N,F cysteine dioxygenase, type I cysteine dioxygenase, type I 25024 1124 E03229 N cysteine dioxygenase, type I cysteine dioxygenase, type I 1203 1049 AJ000485 N cytoplasmic linker 2 cytoplasmic linker 2 17226 1612 Z36980 N,C,E D-dopachrome tautomerase D-dopachrome tautomerase 17227 1612 Z36980 N,E D-dopachrome tautomerase D-dopachrome tautomerase 18354 1559 X59859 J decorin decorin 3279 717 AI103224 F dehydrogenase/reduclase (SDR family) member 4 dehydrogenase/reduclase (SDR family) member 4 19679 1042 AI639418 M,A,D,G,I delodinase lodothyronine, type I deiodinase, iodothyrcnine, type I Table 3 GLGC GenBank Acc or Identifier Seq ID RefSeq ID Model Code Human Homologous Gene Name Human Homologous Cluster Title 19678 1552 X57999 M deiodinase, iodothyronine, typel deiodinase, iodothyronine, type I 20886 1484 U76635 E,G deoxyribonuclease I deoxyribonuclease I 20887 1484 U76635 N,E,G deoxyribonuclease I deoxyribonuclease I 17684 220 AA892345 M,I dimethylglycine dehydrogenase precursor dimethylglycine dehydrogenase precursor 15616 570 AI011996 N DnaJ (Hsp40) homolog, subfamily B, member 9 DnaJ (Hsp40) homolog, subfamily B, member 9 16227 777 AI145177 F early growth response 4 early growth response 4 20865 1175 L00117 M,N elastase 1, pancreatic elastase 1, pancreatic 21562 1525 X15958 N,A enoyl Coenzyme A hydralase, short chain, 1, mitochorndrial enoyl Coenzyme A hydralase, short chain, 1, mitochondrial eukaryotic translation initiation factor 2B, subunit 3 gamma, 797 1452 U38253 N 58kDa eukaryotic translation initiation factor 2B, subunit 3 gamma, 58kDa 1570 1404 U05014 A eukaryotic translation initiation factor 4E binding protein 1 eukaryotic transltation initiation factor 4E binding prolein 1 18713 585 AI012604 N,L eukaryotic translation initiatin factor 5 eukaryotic translation initiation factor 5 18716 1345 NM_020075 F eukaryo5c translation initiation factor 5 eukaryotic translation initiation factor 5 6451 149 AA875033 N fibulin 5 fibulin 5 23445 1310 M84719 M,N flavin containing monooxygenase 1 flavin containing moncoxygenase 1 2242 586 A1012635 M,H,I,J flavin containg moncoxygenase 3 flavin containing moncoxygenase 3 5601 958 A1232461 M,I flavin containing moncoxygenase 4 flavin containing moncoxygenase 4 1143 1343 NM_019280 A gap junction protein, alpha 5, 40kDa (connexin 40) gap juction protein, alpha 5, 40kDa (connexin 40) 617 1179 L08831 N gastric inhibitory polypeptide gastric inhibitory polypeptide 1678 1331 M96674 N glucagon receptor glucagon receptor 11153 1320 M91652 N glutamate-ammonia ligase (gluamine synthase) glutamate-ammonia ligase (glutamine synthase) 5206 327 AA925755 E glutaminase glutaminase 20171 844 AI176504 N glutaminase glutaminase 6405 1208 L38615 G glutathione synthtase glutathione synthetase 6406 1208 L38615 N glutathione synthtase glutathione synthetase 22554 353 AA945076 M,I glycerol kinase glycerol kinase 1550 1504 X06150 N glycin N-methyltransferase glycine N-methyltransferase 1551 1504 X06150 N,G glycine N-methyltransferase glycine N-methyltransferase 17524 559 AI010568 M,A,I growth homone receptor growth hormone receptor 10887 1617 283757 M,I growth hormone receptor growth hormone receptor 1546 1489 U85512 M,N,G GTP cyclohydrolase I fedback regulatory protein GTP cyclohydrolase I feedback regulatory protein 14184 126 AA859837 M guanine deaminase guanine deaminase 14185 126 AA859837 M guanine deaminase guanine deaminase Table 3 GLGC GenBank Acc or Identifier Seq ID RefSeq ID Model Code Human Homologous Gene Name Human Homologous Cluster Title 1246 1273 M57507 M,J guanylale cyclase 1, soluble, beta 2 guanylate cyclase 1, soluble, bela 2 16081 888 Al179610 N heme oxygenase (decycling) 1 heme oxygenase (decycling) 1 16080 1138 J02722 N heme oxygenase (decycling) 1 heme oxygenase (decycling) 1 17832 573 al012182 J hemoglobin, beta hemoglobin, beta 17833 868 al177992 F hemoglobin, beta hemoglobin, beta 17829 884 Al179576 N,J hemoglobin, beta hemoglobin, beta 25468 1324 M94918 N,J hemoglobin, beta hemoglobin, beta 6758 592 Al013394 B,L heparan sulfate (glucosamine) 3-O-sulftransferase 1 heparan sulfate (glucosamine) 3-O-sulfotransferase 1 4235 733 al104524 M,H,K,L heterogeneous nuclear ribonucleoprotein A/B heterogreneous nuclear ribonucleoprotein A/B 16012 1567 X62875 M,I high mobility group AT-hook 1 high mobility group AT-hook 1 15434 531 al008836 N high-mobility group box 2 high mobility group box 2 1437 114 D84418 E high mobility group box 2 high mobility group box 2 3610 776 Al145151 M,G,I,J histamine N-methyltransferase histamine N-methyltransferase 3608 1067 D10693 M,J histamine N-methyltransferase histamine N-methyltransferase 3609 1395 S82579 N,F histamine N-methyltransferase histamine N-methyltransferase 15750 443 AB007690 H homer homolog 2 (Drosophila) homer homolog 2 (Drosophila) 24631 1096 D37951 F human immundeficiency virus type I enhancer binding protein 2 human immundeficiency virus type I enhancer binding protein 2 hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid della hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid della 1962 434 AB000199 isomerase 7 isomerase 7 23660 747 Al105448 N hydroxysleroid (11-beta) dehydrogenase 1 hydroxysleroid (11-beta) dehydrogenase 1 15174 1469 U59809 N insulin-like growth factor 2 receptor insulin-like growth factor 2 receptor 16982 1278 M58634 M,B,L insulin-like growth factor binding protein 1 insulin-like growth factor binding protein 1 15097 535 al009405 N insulin-like growth factor binding protein 3 insulin-like growth factor binding protein 3 24893 614 Al029920 B insulin-like growth factor binding protein 5 insulin-like growth factor binding protein 5 21193 1291 M69055 F insulin-like growth factor binding protein 6 21977 1365 S46785 A,B insulin-like growth factor binding protein acid labile subunit insulin-like growth factor binding protein acid labile subunit 25480 1365 S4678 N insulin-like growth factor binding protein acid labile subunit insulin-like growth factor binding protein acid labile subunit 20126 1263 M34253 N,K interferon regulatory factor 1 interferon regulatory factor 1 17908 604 Al014163 M interferon-related developmental regulator 1 interferon-related developmental regulator 1 2632 456 AB016489 A,D jumping translocation breakpoint jumping translocation breakpoint 3584 716 Al103106 E lamin B1 lamin B1 3049 889 Al179892 M lipocalin 7 lipocalin 7 Table 3 GLGC GenBank Acc or Identifier Seq ID RefSeq ID Model Code Human Homologous Gene Name Human Homologous Cluster Title 3050 939 Al231321 M lipocalin 7 lipocalin 7 low density lipoprotein receptor-related protein associated 408 250 AA892810 M protein 1 low density lipoprotein receptor-realted protein associated protein 1 low density lipoprotein receptor-related protein associated 410 532 Al008974 M,E protein 1 low density lipoprotein receptor-realted protein associated protein 1 low density lipoprotein receptor-related protein associated 409 953 Al232268 M,N,I protein 1 low density lipoprotein receptor-realted protein associated protein 1 low density lipoprotein receptor-related protein associated 406 1606 Z11995 M protein 1 low density lipoprotein receptor-realted protein associated protein 1 low density lipoprotein receptor-related protein associated 407 1606 Z11995 N,C protein 1 low density lipoprotein receptor-realted protein associated protein 1 1946 1338 NM_017061 F lysyl oxidase lysyl oxidase 1943 1388 S77494 N,L lysyl oxidase lysyl oxidase 13151 571 al012030 M matrix gla protein matrix gla protein 7690 1346 NM_022284 M melanoma antigen, family D, 1 melanoma antigen, family D, 1 17357 1317 M88601 M,F,G,I,L meprin A, beta meprin A, beta 16354 1108 D50564 N,C mercaptopyruvale sulfurtransferase mercaptopyruvale sulfurtransferase 15017 1153 J03752 N,B microsomal glutathione S-transferase 1 microsomal glutathione S-transferase 1 13938 1339 NM_017212 N microtubule-associated protein tau microtubule-associated protein tau 13939 1339 NM_017212 D microtubule-associated protein tau microtubule-associated protein tau 13940 1587 X79321 N,D microtubule-associated protein tau microtubule-associated protein tau 25235 1052 AJ001290 F mitochondrial ribostomal protein S6 mitochondrial ribostomal protein S6 14956 1286 M64301 N milogen-activated protein kinase 6 milogen-activated protein kinase 6 14957 1286 M64301 N milogen-activated protein kinase 6 milogen-activated protein kinase 6 15291 748 Al111401 D multiple inositol polyphosphate histidine phosphatease, 1 multiple inositol polyphosphate histidine phosphatease, 1 17448 912 Al229637 N MYB binding protein (P160) 1a MYB binding protein (P160) 1a 1698 1137 J02679 M,B,H,I NAD(P)H dehydrogenase, quinone 1 NAD(P)H dehydrogenase, quinone 1 4484 213 AA892258 N NADPH oxidase 4 NADPH oxidase 4 18008 1350 NM_031588 N neuregulin 1 neuregulin 1 18005 1401 U02320 N neuregulin 1 neuregulin 1 18011 1402 U02322 M,H neuregulin 1 neuregulin 1 20708 441 AB006461 A neurochondrin neurochondrin 968 1119 D86745 G,K nuclear receptor subfamily 0, group B, member 2 nuclear receptor subfamily 0, group B, member 2 Table 3 GLGC GenBank Acc or Identifier Seq ID RefSeq ID Model Code Human Homologous Gene Name Human Homologous Cluster Title 15022 38 AA801029 N nuclear receptor subfamily 2, group F, member 6 nuclear receptor subfamily 2, group F, member 6 1490 1473 U63839 E nucleoporin like 1 nucleoporin like 1 24264 927 Al230712 M paired basic amino acid cleaving system 4 paired basic amino acid cleaving system 4 20457 452 AB012944 M,B,K,I. parathyroid hormone receptor 1 parathyroid hormone receptor 1 24058 1202 L31394 M,I,K,L. parathyroid hormone receptor 1 parathyroid hormone receptor 1 1581 1435 U23769 M,A,C PDZ and LIM dmain 1 (eifin) PDZ and LIM dmain 1 (eifin) 1081 466 AFD13145 M,D PDZ doamin cotaining 1 PDZ doamin cotaining 1 19998 964 Al232999 M PDZ doamin cotaining 1 PDZ doamin cotaining 1 1650 46 AA817825 A peptidylglycine alpha-amidating monooxygenase peptidylglycine alpha-amidating monooxygenase 1644 167 AA891068 A,F peptidylglycine alpha-amidating monooxygenase peptidylglycine alpha-amidating monooxygenase 1649 724 Al103782 F peptidylglycine alpha-amidating monooxygenase peptidylglycine alpha-amidating monooxygenase 1651 896 Al228068 A,H peptidylglycine alpha-amidating monooxygenase peptidylglycine alpha-amidating monooxygenase 1652 914 Al229728 A peptidylglycine alpha-amidating monooxygenase peptidylglycine alpha-amidating monooxygenase 1653 980 Al233806 A peptidylglycine alpha-amidating monooxygenase peptidylglycine alpha-amidating monooxygenase 17477 305 AA924029 M,K,L phospholipid scramblase 1 phospholipid scramblase 1 1847 1592 X16555 B phosphoribosyl pyrophosphate synthetase 2 phosphoribosyl pyrophosphate synthetase 2 6554 517 AF097723 N plasma glutamate carboxyptptidase plasma glutamate carboxyptptidase 46 1242 M23697 N plasminogen activator, tissue plasminogen activator, tissue 19031 666 Al070532 M,L pleckstrin homologylike domain, family A, member 1 pleckstrin homologylike domain, family A, member 1 108 1185 L14002 J polymeric immunoglobuline receptor polymeric immunoglobuline receptor 109 1187 L14004 N polymeric immunoglobuline receptor polymeric immunoglobuline receptor 5295 332 AA926247 M,L potassium channel, subfamily K, member 1 potassium channel, subfamily K, member 1 19665 472 AF022819 D,L potassium channel, subfamily K, member 1 potassium channel, subfamily K, member 1 9027 218 AA892312 N potassium imwardly-rectifying channel, subfamily J, member 16 potassium imwardly-rectifying channel, subfamily J, member 16 (pre-B-cell colony-enhancing factor, similar to Pre-B cell enhancing 14425 864 Al17755 M,L pre-B-cell colony-enhancing factor factor precursor) 5208 1016 Al236754 G pregnancy-induced growth inhibitor pregnancy-induced growth inhibitor 2109 47 AA817887 N,G profilin 1 profilin 1 9067 657 Al070087 M prolactin prolactin 24568 1211 L48060 M,B prolaclin receptor prolaclin receptor 24567 1234 M19304 N,F prolaclin receptor prolaclin receptor 24566 1296 M74152 B,F,L prolaclin receptor prolaclin receptor 1422 450 AB012759 M,B,G,L prolyl endopeptidase prolyl endopeptidase Table 3 GLGC GenBank Acc or Identifier Seq ID RefSeq ID Model Code Human Homologous Gene Name Human Homologous Cluster Title 503 1082 D16443 C prostaglandin E reptor 3 (subtype EP3) prostaglandin E reptor 3 (subtype EP3) 13609 229 AA892468 M,H,I protease, serine, 8 (prostasin) protease, serine, 8 (prostasin) M,A,C,F,H,I, 13610 229 AA892468 K protease, serine, 8 (prostasin) protease, serine, 8 (prostasin) 13611 879 Al79378 M,F,H protease, serine, 8 (prostasin) protease, serine, 8 (prostasin) 1884 1109 D50695 I proteaseom (prosome, macropain) 26S subunit, ATPase, 4 proteaseom (prosome, macropain) 26S subunit, ATPase, 4 15470 1466 U57050 H proteaseom (prosome, macropain) 26S subunit, non-ATPase, 1 proteaseom (prosome, macropain) 26S subunit, non-ATPase, 1 proteaseom (prosome, macropain) 26S subunit, beta type, 9 (large proteaseom (prosome, macropain) 26S subunit, beta type, 9 (large 4003 1071 D10757 N multifunctional protease 2) multifunctional protease 2) 24563 1167 J05592 N,G,K protein phosphatase 1, regulalory (inhibitor) subunit 1A protein phosphatase 1, regulalory (inhibitor) subunit 1A 24564 1167 J05592 N,G,K protein phosphatase 1, regulalory (inhibitor) subunit 1A protein phosphatase 1, regulalory (inhibitor) subunit 1A 21491 486 AF040954 B protein phosphatase 1, regulalory subunit 10 protein phosphatase 1, regulalory subunit 10 1824 1427 U17971K protein tyrosine phosphatase, non-receptor type 21 protein tyrosine phosphatase, non-receptor type 21 24438 1311 M85183 M,N,F,L PYRIN-containg APAF1-like protein 5 PYRIN-containg APAF1-like protein 5 1478 1447 U32314 M pyruvate carboxylase pyruvate carboxylase 1479 1447 U32314 N,D pyruvate carboxylase pyruvate carboxylase 23362 537 Al009605 N Ras homolog enriched in brain Ras homolog enriched in brain 2 4661 296 AA899709 M,B,L recetor (calcitonin) activity modifying protein 3 recetor (calcitonin) activity modifying protein 3 1515 1064 D10233 J renin binding protein renin binding protein 21575 1544 X55298 J ribophorin II ribophorin II 18107 1594 X94242 N ribosomal protein L14 ribosomal protein L14 5667 1553 X58200 N ribosomal protein L23 18611 1553 X58200 N ribosomal protein L23 15135 1382 S71021 N,G ribosomal protein L6 ribosomal protein L6 10878 1174 K03250 N ribosomal protein S11 ribosomal protein S11 20872 1534 X51707 N ribosomal protein S19 15653 1518 X14210 N,G ribosomal protein S4, X-linked 16394 524 al008106 K S100 calcium binding protein A6 (calcyclin) S100 calcium binding protein A6 (calcyclin) 4280 922 Al230247 F selenoprotein P, plasma, 1 selenoprotein P, plasma, 1 serine (or cysteine) proteinase inhibitor, dade A (alpha-1 (hypothelical protein MGC25863, serine (or cysteine) proteinase 699 1463 U55765 E antiproteinase, antitrypsin,) member 10 inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 10) 24778 1515 X13119 N serine dehydralase serine dehydratase Table 3 GLGC GenBank Acc or Identifier Seq ID RefSeq ID Model Code Human Homologous Gene Name Human Homologous Cluster Title 4198 1305 M83143 M,N,I sialyltransferase 1 (beta-galactoside alpha-2,6-sialyltransferase) sialyltransferase 1 (beta-galactoside alpha-2,6-sialyltransferase) 4199 1305 M83143 M,N sialyltransferase 1 (beta-galactoside alpha-2,6-sialyltransferase) sialyltransferase 1 (beta-galactoside alpha-2,6-sialyltransferase) solute carrier family 13 (sodium-dependent dicarboxylate solute carrier family 13 (sodium-dependent dicarboxylate 17500 243 AA892616 N transporter), member 3 transporter), member 3 235 1344 NM_019347 C solute carrier family 14 (urea transporter), member 2 solute carrier family 14 (urea transporter), member 2 15039 951 Al232096 M,F,I solute carrier family 15 (H+/peptide transporter), member 2 solute carrier family 15 (H+/peptide transporter), member 2 solute carrier family 16 (monocarboxylic acid transporters), solute carrier family 16 (monocarboxylic acid transporters), member 725 1471 U62316 B member 7 7 Table 3 GLGC GenBank Acc or Identifier Seq ID RefSeq ID Model Code Human Homologous Gene Name Human Homologous Cluster Title 15872 1201 L28135 N solute carrier family 2 (familtated glucose transporter), member 2 solute carrier family 2 (familtated glucose transporter), member 2 1510 440 AB004559 M,D,K solute carrier family 22 (organic anion transporter), member 6 solute carrier family 22 (organic anion transporter), member 6 12682 797 Al169656 D solute carrier family 22 (organic anion transporter), member 8 solute carrier family 22 (organic anion transporter), member 8 1602 1483 U76379 N solute carrier family 22 (organic cation transporter), member 1 solute carrier family 22 (organic cation transporter), member 1 770 112 D83044 M,N solute carrier family 22 (organic cation transporter), member 2 solute carrier family 22 (organic cation transporter), member 2 23625 458 AB017260 N,D solute carrier family 22 (organic cation transporter), member 5 solute carrier family 22 (organic cation transporter), member 5 43 1194 L23413 N solute carrier family 26 (sulfate transporter), member 1 solute carrier family 26 (sulfate transporter), member 1 17554 1115 D85100 N solute carrier family 27 (fatty acid transporter), member 2 solute carrier family 27 (fatty acid transporter), member 2 18074 469 AF015305 K solute carrier family 29 (nucleoside transporters), member 2 solute carrier family 29 (nucleoside transporters), member 2 6416 984 Al234295 M,K solute carrier family 34 (sodium phosphate), member 2 solute carrier family 34 (sodium phosphate), member 2 20780 1444 U29881 M,N,D solute carrier family 5 (sodium/glucose cotransporter), member 2 solute carrier family 5 (sodium/glucose cotransporter), member 2 7700 744 Al105383 M,D sphingosne kinase 1 sphingosne kinase 1 splicing factor proline/glutamine rich (polypyrimidine tract binding splicing factor proline/glutamine rich (polypyrimidine tract binding 8426 483 AF036335 N,E,F protein associated) protein associated) 16681 1095 D37920 N,B,L squalene epoxidase squalene epoxidase 21842 828 Al172293 N sterol-C4-methyl oxidase-like sterol-C4-methyl oxidase-like 14970 180 AA891738 M,B,H,I,K sulfite oxidase sulfite oxidase 11692 1027 Al638982 M,N sulfotransferase family, cytosolic, 1C, member 1 sulfotransferase family, cytosolic, 1C, member 1 495 1573 X68041 J superoxide dismutase 3, extracellular superoxide dismutase 3, extracellular 494 1610 Z24721 J superoxide dismutase 3, extracellular superoxide dismutase 3, extracellular 21025 111 AA859241 M,A,C synaptojanin 2 binding protein synaptojanin 2 binding protein 21024 1348 NM_022599 M synaptojanin 2 binding protein synaptojanin 2 binding protein 15247 606 Al014169 N thioredoxin interacting protein thioredoxin interacting protein 20816 1276 M58404 M,G,K thymosin, beta 10 thymosin, beta 10 7888 976 al233583 M tissue inhibitor of metalloproteinae 2 tissue inhibitor of metalloproteinae 2 17149 1304 M83107 N transgelin transgelin 17150 1304 M83107 N transgelin transgelin 17550 565 Al011607 M,I trimethyllysine hydroxylase, epsilon trimethyllysine hydroxylase, epsilon 14332 1051 AJ001044 D tumor-associated calcium signal transducer 1 tumor-associated calcium signal transducer 1 tyrosine 3-monooxygenase/tryplophan 5-monooxygenase tyrosine 3-monooxygenase/tryplophan 5-monooxygenase activation 16683 1086 D17445 N activation protein, eta polypeptide protein, eta polypeptide Table 3 GLGC GenBank Acc or Identifier Seq ID RefSeq ID Model Code Human Homologous Gene Name Human Homologous Cluster Title tyrosine 3-monooxygenase/tryptophan 5-monooxygenase tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation 16684 1086 D17445 M activation protein, eta polypeptide protein, eta polypeptide 3016 50 AA818069 H ubiquitin B ubiquitin B 3015 1084 D16554 A ubiquitin B ubiquitin B 11843 494 AF054826 A vesicle-associated membrane protein 5 (myobrevin) vesicle-associated membrane protein 5 (myobrevin) 15185 1568 X62952 M wimentin wimentin 15008 485 AF038591 E X-prolyl aminopeptidase (aminopeptidase P) 1, soluble X-prolyl aminopeptidase (aminopeptidase P) 1, soluble X-prolyl aminopeptidase (aminopeptidase P) 2, membrane- 12331 370 AA946466 M,H bound X-prolyl aminopeptidase (aminopeptidase P) 2, membrane-bound X-prolyl aminopeptidase (aminopeptidase P) 2, membrane- 13332 370 AA946466 M,G bound X-prolyl aminopeptidase (aminopeptidase P) 2, membrane-bound 1410 1330 M96548 H zinc finger protein 354A zinc finger protein 354A 22501 351 AA944811 H zinc finger, DHHC domain containing 7 zinc finger, DHHC domain containing 7 22502 608 Al029017 H zinc finger, DHHC domain containing 7 zinc finger, DHHC domain containing 7 Table 4 GLGC Model GLGC Model Code Table No. General Nephrotoxicity M (GENERAL1)* 5M General Nebhrotoxicity N (GENERAL2)** 5N Chloroform A 5A Diclofenac B 5B Menadione C 5C SodiumChromate D 5D SodiumOxalate E 5E Thioacetamide F 5F Vancomycin G 5G proximal tubule S2 segment toxicity H 5H Tubular Toxicity I 5I Glomerular njuryJ 5J Tubular Obstruction K 5K NSAIDS L 5L * MAS4 LDA Based ** RMA PLS Based Table 5A GLGC Identifier LDA Score Tox Group Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 3091 95. 09 421. 64 58. 81 713. 53 158. 43 4462 93. 09 414. 41 198. 64 953. 78 313. 55 22648 92. 73 313. 31 70. 15 490. 37 101. 26 13610 92. 33 226. 14 59. 71 365. 06 107. 29 21025 92. 15 233. 83 71. 17 418. 06 106. 83 3961 91. 61 74. 40 10. 55 49. 45 14. 81 2912 90. 89 1436. 37 179. 76 2437. 60 603. 29 17361 90. 70 50. 93 20. 08 137. 86 55. 93 23509 89. 88 1570. 55 137. 71 2086. 99 379. 49 13028 89. 85 137. 00 17. 66 89. 57 32. 90 20725 88. 97 621. 86 57. 64 801. 80 141. 09 11953 88. 88 1079. 47 146. 45 1693. 94 588. 62 1652 88. 73 476. 16 64. 04 656. 76 161. 47 4463 88. 62 43. 16 34. 48 150. 98 58. 66 25643 88. 48 187. 37 74. 36 110. 76 25. 22 3875 88. 29 252. 35 75. 16 478. 18 126. 13 16469 88. 06 991. 10 103. 75 1321. 05 271. 57 1650 87. 97 569. 84 94. 38 790. 48 182. 69 8829 87. 88 505. 66 151. 99 282. 86 84. 70 23282 87. 61 425. 15 71. 15 283. 98 52. 36 9191 87 55 277. 28 132. 99 657. 06 277. 10 13727 87. 53 35. 36 28. 82 109. 18 42. 58 15032 87. 42 175. 94 47. 04 265. 22 74. 56 2059 87. 30 219. 06 65. 06 136. 38 34. 61 21088 87. 30 56. 92 8. 06 40. 35 14. 32 18522 87. 29 490. 66 94. 81 759. 01 194. 27 21977 87. 24 38. 53 11. 16 77. 01 45. 15 11653 87. 24 306. 58 112. 65 560. 40 195. 77 23033 87. 21 431. 39 57. 07 579. 07 117. 99 19822 86. 82 994. 53 147. 26 1418. 54 381. 93 9176 86. 73 288. 61 15. 81 245. 52 51. 27 17524 86. 71 799. 10 105. 47 1115. 60 282. 08 7216 86. 71 123. 29 34. 23 234. 44 71. 10 11761 86. 64 49. 48 6. 15 68. 95 26. 33 4473 86. 50 95. 76 32. 22 172. 47 49. 25 3925 86. 50 275. 69 80. 34 461. 73 112. 55 14856 86. 45 330. 60 53. 33 438. 34 100. 70 2439 86. 44 102. 63 17. 35 147. 69 27. 96 22490 86. 42 811. 57 139. 35 602. 93 96. 00 14267 86. 42 1171. 51 258. 92 1706. 75 393. 91 8927 86. 42 508. 53 79. 40 689. 86 154. 77 8946 86. 39 112. 12 21. 59 186. 07 74. 49 4178 86. 29 444. 39 54. 78 619. 34 136. 02 23115 86. 26 278. 57 65. 22 503. 85 159. 60 16958 86 15 61. 46 19. 84 30. 96 13. 91 9116 86. 14 269. 31 52.99 392.85 75. 60 15836 86. 00 121. 07 16. 96 214. 57-101. 58 13285 85. 94 110. 31 17. 04 71. 38 16. 98 5369 85. 88 274. 28 47. 68 200. 95 43. 34 8721 85. 83 73. 87 43. 04 183. 86 66. 21 3803 85. 73 975. 63 205. 56 722. 11 154. 02 1409 85. 68 298. 20 49. 00 438. 84 99. 15 17824 85. 62 205. 14 27. 09 142. 57 42. 17 7299 85. 42 334. 53 109. 96 181. 79 143. 50 Table 5A GLGC Identifier LDA Score Tox Group Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 1653 85. 35 686. 13 93. 92 993. 47 242. 55 17516 85. 33 500. 55 239. 88 547. 02 127. 42 19377 85. 21 155. 74 30. 08 109. 47 24. 61 1570 85. 17 98. 50 59. 57 39. 00 13. 49 1651 85. 17 577. 75 69. 32 788. 50 180. 99 7622 85. 09 88. 74 20.90 56.95 16. 90 22855 85. 05 373. 13 49. 91 519. 30 117. 46 21562 85. 05 265. 87 68. 99 468. 38 147. 67 4933 84. 98 743. 88 516. 81 142. 53 232. 49 15964 84. 88 583. 51 205. 70 1089. 69 286. 46 24234 84. 86 408. 25 208. 57 188. 66 107. 50 7634 84. 86 538. 91 181. 95 645. 21 126. 88 12129 84. 85 245. 65 111. 61 646. 79 334. 57 25777 84. 83 1173. 74 710. 54 439. 45 241. 72 10378 84. 82 69. 21 33. 23 143. 74 101. 86 1581 84. 77 87. 66 15. 15 66. 76 21. 00 20582 84. 74 347. 72 63. 49 487. 44 95. 49 20000 84. 67 93. 69 19. 60 127. 60 71. 39 13740 84. 64 257. 51 18. 03 221. 70 39. 96 16756 84. 59 361. 18 150. 11 171. 51 41. 28 26183 84. 58 64. 68 11. 03 47. 22 22. 02 22985 84. 55 83. 55 9. 87 108. 90 29. 86 23718 84. 42 65. 41 10. 03 97. 59 40. 96 10130 84. 36 117. 70 66. 31 221. 33 55. 16 17541 84. 35 1464. 81 514. 58 725. 03 344. 90 21060 84. 30 133. 69 25. 56 83. 14 27. 48 16468 84. 29 831. 97 118. 43 1136. 11 219. 87 20741 84. 26 236. 26 31. 17 175. 32 43. 96 6641 84. 21 233. 86 84. 82 396. 94 88. 30 22537 84. 18 145. 19 78. 83 301. 55 137. 94 18509 83. 95 311. 54 43. 78 430. 03 88. 77 19110 83. 92 84. 32 32. 08 204. 53 96. 17 11843 83. 88 61. 43 4. 65 52. 11 10. 69 15800 83. 74 56. 84 10. 37 34. 45 19. 58 7936 83. 74 93. 98 18. 72 137. 68 31. 48 22783 83. 67 473. 86 73. 76 347. 89 212. 99 20832 83. 65 534. 47 85. 79 785. 26 199. 66 1949 83. 61 57. 75 7. 72 90. 12 37. 12 21061 83. 52 86. 99 17. 50 50. 51 22. 34 25168 83. 29 32. 68 2. 87 23. 16 9. 80 6127 83. 24 41. 36 8. 04 64. 30 27. 81 19679 83. 24 440. 67 183. 93 755. 52 202. 10 15701 83. 20 63. 42 22. 84 30. 93 12. 46 20896 83. 09 106. 66 65. 89 141. 12 40. 19 13646 82. 98 1169. 38 295. 87 817. 10 184. 73 6343 82. 92 46. 79 4. 81 34. 28 11. 62 1877 82. 89 444. 75 101. 68 652. 86 170. 37 24437 82. 76 56. 38 5. 77 61. 94 29. 69 16948 82. 71 145. 85 69. 01 317. 13 132. 79 825 82. 62 22. 20 8. 99 46. 45 18. 16 25862 82. 39 38. 61 8. 30 23. 01 10. 20 1143 82. 38 131. 83 21. 57 92. 25 32. 27 20708 82. 38 80. 85 9. 57 61. 19 17. 28 20833 82 32 1010. 33 178. 76 1449. 79 326. 39 Table 5A GLGC Identifier LDA Score Tox Group Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 19144 82. 32 36. 63 8. 07 25. 15 10. 80 2632 82. 26 190. 41 17. 08 153. 91 30. 61 1644 82. 23 418. 83 62. 93 560. 68 126. 32 3015 82. 18 2837. 91 186. 68 2819. 00 1012. 99 7505 81. 98 274. 29 43. 54 384. 55 118. 76 1509 81. 62 431. 65 81. 24 550. 73 118. 16 25921 81.56 47. 30 10. 74 28. 36 16. 07 1460 81. 41 281. 25 87. 21 192. 24 83. 91 1929 81. 33 536. 97 208. 01 870. 13 215. 86 9905 81.30 538. 90 116.34 744.96 153. 52 15072 81. 24 42. 04 6. 55 31. 15 15. 09 Table 5B GLGC Identifier LDA Score Tox Group Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 7540 97. 91 504. 78 145. 39 158. 51 83. 92 8820 97. 91 743. 55 284. 97 139. 15 119. 88 7299 97. 61 595. 57 144. 70 180. 65 140. 60 5920 97. 46 1412. 80 271. 66 635. 94 191. 82 24200 97. 01 885. 64 139. 99 426. 56 138. 77 17805 96. 58 1504. 75 444. 21 682. 13 328. 81 4661 96. 19 555. 94 110. 43 307. 06 85. 59 15964 95. 49 487. 88 126. 89 1089. 29 286. 36 24197 95. 31 82. 06 26. 90 235. 59 79. 78 15411 94. 83 552. 53 112. 91 304. 39 94. 23 8065 94. 80 236. 57 31. 67 163. 82 37. 32 21977 94. 77 30. 72 6. 14 76. 98 45. 11 725 94. 04 33. 60 10. 05 110. 06 46. 60 14450 93. 98 45. 80 9. 30 146. 93 73. 46 7936 93. 59 82. 66 12. 40 137. 66 31. 43 4330 93. 19 242. 18 59. 53 461. 51 139. 37 21012 92. 66 445. 05 162. 22 203. 66 116. 06 6046 92. 65 83. 37 33. 70 193. 87 62. 20 3465 92. 50 152. 39 23. 63 263. 07 79. 12 15017 92. 48 2241. 27 415. 11 1149. 81 399. 55 7872 92. 44 63. 92 8. 33 112. 60 35. 96 21014 92. 42 352. 43 145. 68 149. 67 82. 43 19067 92. 38 76. 83 28. 49 162. 21 46. 61 8234 92. 38 22. 24 6. 70 47. 07 15. 98 5461 91. 99 694. 84 296. 55 199. 69 117. 96 22311 91. 96 1255. 02 184. 06 688. 00 158. 37 17541 91. 84 1839. 84 669. 37 724. 33 339. 91 16982 91. 81 1036. 49 606. 21 130. 48 296. 12 7937 91. 71 34. 46 21. 21 176. 64 93. 91 15679 91. 36 309. 12 62. 83 174. 14 47. 36 15125 91. 33 3102. 06 1017. 25 1525. 20 405. 25 665 91. 27 849. 30 217. 79 538. 96 94. 94 6278 91. 08 58. 48 10. 10 94. 99 25. 06 14970 90. 99 134. 42 36. 31 199. 60 41. 02 3172 90. 74 36. 28 40. 56 206. 90 111. 79 8104 90. 62 85. 37 9. 09 60. 70 24. 71 23151 90. 62 204. 97 55. 56 355. 14 101. 19 14346 90. 51 174. 62 63. 19 52. 54 90. 15 5930 90. 51 73. 85 24. 31 26. 85 19. 94 1698 90. 48 190. 91 66. 62 70. 39 93. 92 11755 90. 42 343. 83 127. 98 144. 25 136. 11 6014 90. 36 183. 73 46. 62 80. 51 44. 34 16898 90. 26 55. 03 10. 77 78. 17 16. 44 14595 90. 21 167. 82 59. 62 77. 65 33. 41 17401 90. 15 1909. 24 588. 72 1010. 74 422. 89 10446 90. 14 22. 58 15. 15 127. 88 91. 52 13614 90. 06 497. 29 91. 75 324. 4 71. 36 15189 90. 00 4842. 58 1706. 56 2020. 75 1168. 41 15035 89. 99 23. 84 16. 64 124. 98 68. 66 13966 89. 97 227. 19 38. 65 159. 84 32. 03 10434 89. 97 77. 07 35. 03 33. 65 20. 30 1340 89. 87 124. 95 20. 55 184. 83 85. 84 8850 89. 82 175. 34 58. 83 99. 07 34. 66 16521 89. 73 453. 74 109. 04 284. 15 76. 30 Table 5B GLGC Identifier LDA Score Tox Group Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 12921 89.73 213.56 56.93 102.59 48. 69 13013 89. 59 32. 49 10. 44 65. 57 21. 46 6758 89. 57 59. 84 19. 18 28. 92 13. 70 22885 89. 51 2441. 02 725. 57 1292. 56 483. 73 20831 89. 50 55. 62 17. 29 138. 12 57. 86 21354 89. 39 640. 85 156. 38 418. 77 127. 04 12979 89. 39 742. 50 248. 93 366. 97 196. 56 11991 89. 35 20. 14 10. 16 46. 26 16. 40 6796 89. 30 304. 75 71. 31 192. 78 51. 24 21976 89. 24 462. 91 64. 44 316. 41 69. 92 20523 89. 18 1004. 68 208. 03 579. 32 164. 47 21975 89. 03 357. 73 79. 92 212. 58 62. 99 9520 89. 02 69. 60 25. 47 140. 86 46. 37 6917 88. 81 111. 53 14. 34 176. 04 69. 10 8888 88. 78 22. 26 7. 29 48. 79 20. 58 1527 88. 63 51. 23 9. 78 88. 23 39. 31 22479 88. 52 693. 29 140. 68 417. 80 129. 01 8099 88. 52 72. 23 24. 65 43. 64 14. 56 12925 88. 48 44. 20 4. 65 69. 36 29. 98 9079 88. 46 1099. 28 237. 43 736. 13 163. 45 1858 88. 43 253. 42 73. 25 153. 78 50. 88 26083 88. 38 403. 60 200. 12 1199. 39 721. 99 8759 88. 36 237. 31 41. 30 156. 57 41. 79 16520 87. 97 174. 46 63. 58 88. 91 110. 98 24566 87. 61 32. 95 21. 32 180. 03 89. 43 1422 87. 45 174. 39 46. 71 300. 07 105. 44 20864 87. 40 3112. 64 637. 13 1921. 03 633. 85 17088 87. 37 98. 27 17. 79 58. 55 31. 41 25106 87. 02 28. 05 3. 19 38. 61 13. 12 3439 86. 94 135. 79 26. 09 92. 94 24. 52 20405 86. 92 133. 28 70. 23 29. 80 29. 59 21145 86. 79 76. 23 47. 54 200. 42 66. 53 2128 86. 56 97. 35 47. 36 32. 61 16. 44 4449 86. 33 156. 15 44. 78 243. 11 70. 20 24893 86. 30 20. 58 18. 68 85. 55 52. 17 23987 86. 20 596. 80 251. 48 276. 13 75. 22 11434 86. 18 181. 39 56. 52 324. 42 119. 03 1847 86. 15 22. 26 10. 03 62. 17 36. 21 20457 86. 13 235. 87 68. 78 395. 90 100. 59 21491 86. 07 67. 51 10. 34 100. 55 23. 55 24232 85. 94 48. 69 39. 24 151. 29 60. 27 15379 85. 72 33. 32 11. 21 67. 90 28. 41 16681 85. 68 134. 46 57. 78 63. 59 25. 88 15761 85. 67 22. 22 16. 23 77. 85 34. 65 13542 85. 67 321. 75 219. 70 462. 35 148. 34 24568 85. 63 78. 30 23. 68 153. 33 67. 67 1729 85. 55 81. 89 44. 56 212. 81 80. 84 13485 85. 51 38. 32 7. 99 57. 48 16. 43 67 85. 37 1551. 30 178. 56 1151. 89 254. 88 6782 85. 13 310. 65 67. 44 219. 45 62. 29 22321 85. 13 138. 89 29. 75 94. 97 68. 63 15124 85. 11 1897. 22 536. 70 1048. 98 283. 10 954 84. 94 54. 36 5. 77 71. 54 20. 36 189484. 89 294. 35 70. 10 198. 20 72. 90 Table 5B GLGC Identifier LDA Score Tox Group Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 1888 84. 83 101. 45 32. 01 52. 26 33. 35 20682 84. 77 226. 38 89. 62 409. 19 108. 15 18246 84. 64 100. 99 77. 72 258. 41 95. 94 20000 84. 61 24. 08 20. 83 127. 92 70. 97 11481 84. 61 20. 44 15. 73 65. 86 29. 15 1529 84. 43 194. 31 45. 08 294. 86 70. 18 14003 84. 35 1575. 92 414. 94 932. 50 241. 80 18597 84. 32 987. 07317. 42563. 12200. 20 20803 84. 29 737. 50 199. 95 473. 34 124. 77 Table 5C GLGC Identifier LDA Score Tox Group Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 17734 98. 79 321. 98 49. 82 114. 29 102. 66 18642 98. 09 492. 19 42. 17 881. 32 192. 80 21388 97. 24 104. 79 11. 52 27. 72 24. 11 16907 96. 36 33. 38 19. 54 131. 32 51. 03 24042 95. 76 73. 75 40. 11 21. 09 79. 30 22101 95. 58 21. 93 23. 56 170. 51 83. 23 12343 95. 55 89. 32 12. 94 50. 29 16. 25 16948 95. 36 125. 57 23. 36 317. 27 132. 70 1141 95. 33 394. 51 55. 69 241. 23 66. 76 8664 95. 29 1388. 21 550. 83 89.50 215. 23 7142 95.27 363. 26 34. 37 610. 43 144. 19 8665 95. 26 2691. 53 1101. 20 343. 63 497. 74 1475 95. 17 2063. 49 658. 77 155. 80 379. 29 16354 95. 03 20. 78 35. 33 279. 68 148. 90 3863 94. 79 122. 87 17. 81 196. 59 86. 02 12561 94. 73 64. 62 15. 14 148. 52 51. 53 18288 94. 67 217. 71 34. 85 124. 55 43. 60 21029 94. 64 126. 09 12. 20 81. 52 23. 49 24649 94. 42 65. 78 19. 06 112. 21 22. 95 1409 94. 27 290. 95 26. 81 438. 89 99. 13 6290 94. 18 167. 05 14. 13 232. 79 37. 78 17735 94. 05 363. 65 53. 62 178. 33 104. 47 11618 94. 03 224. 46 33. 16 380. 82 110. 84 14083 93. 91 297. 20 43. 33 473. 74 100. 64 16518 93. 89 2054. 01385. 94949. 88306. 74 10004 93.55 78. 40 13. 45 39. 38 19. 65 3474 93. 52 345. 67 22. 76 483. 73 104. 79 1764 93. 42 138. 74 17. 01 88. 17 27. 95 17570 93. 36 379. 60 47. 99 240. 61 81. 89 21672 93. 27 447. 28 37. 64 314. 18 77. 63 23758 93. 24 103. 71 16. 35 174. 80 41. 71 7586 93. 24 455. 38 78. 29 769. 55 187. 42 809 93. 23 100. 66 16. 68 39. 56 39. 66 17938 93. 15 319. 01 21. 59 447. 84 95. 68 22412 93. 08 196. 70 39. 42 91. 13 45. 28 11559 93. 06 318. 5760. 32552. 63125. 46 7300 93. 06 545. 82 63. 96 744. 66 285. 54 22415 92. 95 375. 76 48. 28 206. 41 158. 59 21400 92. 85 211. 40 61.58 361.76 72. 81 20161 92. 68 128. 82 47. 99 32. 65 31. 21 25547 92. 64 407. 00 28. 91 267. 96 104. 45 9116 92. 64 273. 80 27. 04 392. 81 75. 75 12551 92. 58 95. 87 15. 38 164. 16 42. 22 3091 92. 52 531. 24 38. 99 712. 74 159. 66 5565 92. 52 206. 09 47.75 389.83 117. 52 21990 92. 48 28. 82 20.42 121.58 57. 45 25606 92. 45 66. 28 8. 55 40. 17 15. 01 16003 92. 45 198. 48 23. 57 334. 94 104. 96 7049 92. 42 153. 66 20. 90 227. 04 46. 15 18350 92. 35 276. 28 122. 54 92. 32 51. 93 503 92. 18 150. 85 14. 24 103. 15 29. 15 20173 92. 18 32. 74 11. 51 77. 29 31. 95 17755 92.18 246. 88 32. 61 383. 76 97. 58 1460 92. 12 251. 67 29. 18 192. 46 84. 37 Table 5C GLGC Identifier LDA Score Tox Group Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 24672 92. 12 65. 39 7. 99 39. 44 14. 11 10667 92. 09 94. 44 15. 07 38. 95 41. 37 6632 92. 08 270. 94 30. 65 167. 71 54. 30 6736 92. 06 131. 85 22. 79 69. 09 33. 18 6675 92. 06 362. 12 33. 19 548. 28 144. 52 19768 92. 02 1218. 83 166. 71 787. 22 172. 80 3698 91. 97 66. 85 13. 21 128. 16 41. 97 9583 91. 92 154. 31 44. 35 55. 84 61. 67 7936 91. 91 84. 99 15. 68 137. 74 31. 39 6595 91. 85 109. 39 17. 61 68. 80 30. 49 1581 91. 79 87. 16 7. 56 66. 76 21. 04 2824 91. 79 65. 68 9. 52 100. 88 21. 89 19040 91. 74 323. 49 86.16 184.44 121. 72 23834 91. 74 142. 01 30. 15 74. 82 24. 22 23033 91. 64 422. 53 36. 80 579. 14 117. 96 21025 91. 61 267. 66 41. 37 417. 82 107. 31 4952 91. 59 200. 30 34. 51 106. 14 44. 92 21211 91. 55 548. 25 69. 20 850. 78 217. 13 22413 91. 53 141. 51 32. 80 68. 54 38. 43 8837 91. 52 234. 73 29. 31 331. 74 63. 42 21653 91. 50 363. 77 66. 02 237. 45 68. 10 4462 91. 48 567. 85 100. 01 952. 66 315. 50 12450 91. 48 35. 96 20. 64 127. 75 69. 86 11162 91. 45 324. 91 48. 59 495. 59 118. 35 2555 91. 44 145. 97 22. 76 85. 01 42. 88 605 91. 39 38. 02 5. 26 21. 20 10. 90 15138 91. 39 196. 35 69. 14 471. 14 175. 95 25379 91. 38 117. 64 16. 80 71. 75 25. 39 235 91. 30 320. 65 25. 66 230. 34 61. 53 1929 91. 29 473. 25 68. 26 870. 59 215. 67 17256 91. 27 259. 66 52. 16 429. 33 122. 40 24459 91. 21 398. 68 40. 21 276. 39 76. 14 13610 91. 17 219. 12 31. 55 365. 11 107. 30 35 91. 15 784. 74 75. 75 1207. 71 355. 24 12016 91. 15 252. 53 37. 75 465. 80 181. 24 21683 91. 05 65. 76 22. 22 27. 27 20. 99 1501 91. 02 99. 81 25. 56 52. 93 56. 99 25747 90. 98 80. 78 19. 33 42. 91 38. 40 23166 90. 98 229. 86 42. 08 126. 92 62. 06 25279 90. 97 751. 86 61. 65 549. 26 116. 47 9224 90. 94 418. 49 23. 57 559. 20 140. 71 4542 90. 94 270. 11 21. 67 180. 81 56. 07 21696 90. 92 282. 32 32. 07 175. 33 47. 74 20753 90. 89 184. 62 20. 62 119. 99 28. 26 433 90. 88 134. 41 23. 78 80. 86 34. 13 19251 90. 88 562. 71 31. 16 694. 44 105. 77 16469 90. 82 1028. 80 54. 62 1320. 78 271. 98 15791 90. 79 201. 52 56. 18 123. 78 84. 57 17226 90. 79 433. 99 33. 61 577. 07 118. 33 15421 90. 70 562. 11 32. 28 738. 52 153. 62 20085 90. 68 375. 42 39. 17 247. 93 59. 19 407 90. 64 264. 48 35. 26 395. 09 94. 07 17426 90. 61 429. 40 38. 59 568. 65 91. 40 2098 90. 58 232. 32 22. 55 177. 21 39. 37 Table 5C GLGC Identifier LDA Score Tox Group Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 13005 90. 56 143. 19 30. 68 80. 63 29. 18 25098 90. 52 176. 46 75. 02 35. 80 33. 18 10241 90. 38 114. 02 25. 12 59. 17 24. 28 23679 90. 38 78. 01 14. 28 38. 29 19. 90 1652090. 36 123. 97 17.89 89.12 111.29 Table 5D GLGC Identifier LDA Score Tox Group Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 15291 97. 74 227. 69 93. 17 97. 65 27. 73 7896 97. 71 173. 75 8. 10 283. 20 65. 35 3631 97. 59 146. 49 9. 89 93. 75 22. 59 2232 97. 16 36. 74 0. 82 24. 79 11. 77 23626 97. 10 201. 76 49.28 78.54 37. 73 24762 97.07 206. 67 49. 31 926. 38 314. 75 3493 96. 95 123. 15 24. 99 61. 58 18. 38 16625 96. 89 237. 89 5. 08 180. 96 38. 01 11959 96. 86 62. 2510. 64125. 4027. 59 15027 96.86 228. 67 10. 97 139. 90 39. 67 16338 96.77 97. 00 8. 89 58. 64 16. 37 5901 96. 74 159. 91 19. 26 91. 66 42. 91 2423 96. 59 192. 07 14. 10 132. 98 27. 14 12797 96.56 166. 69 40.58 73.77 27.51 11558 96. 56 70. 08 17. 91 160. 77 43. 05 2534 96. 56 68. 06 11. 48 35. 59 11. 40 23790 96.53 123. 00 38. 12 63. 08 19. 14 16859 96.50 245. 89 56. 54 122. 60 47. 46 23698 96. 41 147. 28 9. 50 275. 19 124. 72 16824 96. 41 72. 56 17. 91 227. 30 79. 50 17223 96. 41 1104. 50 35. 58 868. 15 118. 29 2113 96. 38 222. 44 37. 93 132. 53 29. 47 18418 96.35 370. 51 71. 34 245. 92 41. 02 23843 96. 32 187. 45 30. 50 103. 55 28. 14 21659 96.32 386. 36 74.64 204.80 61. 71 22538 96.29 172. 72 15. 27 339. 80 93. 47 12129 96. 29 143. 53 31. 03 645. 40 334. 58 15232 96.26 257. 50 24. 61 169. 53 35. 85 17523 96.17 123. 97 10. 52 81. 13 19. 15 5290 96. 17 22. 52 4. 12 50. 65 15. 13 19152 96. 14 320. 13 96. 93 160. 67 53. 93 22180 96.14 145. 82 40. 45 88. 52 23. 95 8721 96. 14 35. 66 23.53 183.51 66.31 19412 96. 11 219. 32 2. 99 183. 37 50. 07 7700 96. 11 135.98 23.23 80.56 43. 28 24592 96. 05 74. 35 27. 61 329. 43 142. 17 23018 96.05 150. 06 18. 94 105. 15 19. 40 7270 96. 02 267. 75 28. 36 171. 64 36. 71 15159 96. 02 419. 08 74. 41 872. 31 214. 06 22770 95. 99 460. 9161. 30293. 3460. 75 13106 95. 99 68. 92 9.31 37.20 21. 98 22537 95.96 40. 88 34. 27 301. 20 137. 68 14332 95.90 951. 74 99. 04 604. 90 155. 26 17419 95.90 336. 07 70. 94 197. 65 45. 14 17468 95. 87 240. 19 29. 50 414. 57 80. 60 20829 95.84 1805. 57 324. 13 925. 21 315. 25 19469 95.84 134. 02 40. 80 367. 99 99. 90 12673 95. 84 106. 88 41. 08 40. 72 22. 46 18095 95.84 1118. 60 126. 43 801. 84 125. 83 19665 95.81 204. 31 35. 07 88. 59 51. 54 2348 95. 81 97. 18 36. 13 463. 64 200. 40 13940 95. 72 100. 29 27. 43 216. 02 51. 74 12682 95. 62 511. 62 150.58 1734.71 588. 20 13157 95. 59 99. 31 44. 78 328. 67 105. 58 Table 5D GLGC Identifier LDA Score Tox Group Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 15277 95. 56 1199. 28 124. 15 856. 07 134. 65 6055 95. 56 447. 44 133. 36 1045. 52 255. 69 3145 95. 56 152. 93 22. 06 426. 44 138. 00 16731 95. 53 164. 04 17. 44 86. 12 38. 17 1431 95. 53 84. 3635. 10462. 05168. 52 3934 95. 50 716. 78 83. 73 1225. 51 254. 53 15339 95. 47 139. 74 20. 03 227. 15 74. 31 21959 95. 41 234. 36 36. 74 132. 11 42. 91 13104 95. 32 217. 32 35. 96 479. 57 130. 05 15246 95. 23 104. 02 19. 45 63. 14 17. 15 12355 95. 20 55. 04 2. 97 32. 72 17. 38 6869 95. 20 79. 10 7. 52 32. 43 29. 17 23839 95. 17 215. 43 62. 86 469. 65 119. 97 11615 95. 14 539. 91 16. 66 412. 37 87. 18 1479 95. 11 92. 37 36. 66 221. 32 62. 74 2107 95. 11 260. 72 38. 29 437. 31 95. 82 19268 95. 08 1507. 38 104. 73 1082. 49 316. 16 21587 95. 08 63. 47 12. 04 184. 59 76. 44 8215 95. 08 916. 05 104. 30 1510. 03 332. 10 14353 95. 05 92. 56 11. 29 55. 60 17. 26 17378 95. 02 212. 42 29. 92 131. 90 39. 98 6629 95. 02 314. 7737. 87540. 04121. 47 12095 94. 99 365. 17 58. 23 1298. 24 810. 83 8739 34. 99 97. 84 18. 34 265. 76 118. 29 25377 94. 93 56. 11 8. 35 26. 88 13. 79 1510 94. 93 412. 23 94. 86 837. 44 225. 06 19347 94. 93 82. 73 6. 92 47. 68 20. 04 23307 94. 90 142. 12 10. 93 93. 63 26. 00 18524 94. 90 410. 60 75. 64 697. 54 141. 17 24615 94. 84 1270. 53 105. 47 933. 13 210. 70 17823 94. 84 683. 68 66. 28 459. 89 95. 30 1511 94. 81 28. 36 22. 05 333. 19 206. 19 989 94. 78 38. 30 12. 87 147. 38 60. 50 12276 94. 78 72. 82 16. 26 186. 84 61. 45 19936 4. 78 417. 94 86. 08 787. 51 166. 53 5297 94. 75 143. 95 30. 44 352. 41 109. 46 19679 94. 75 329. 18 166. 41 754. 53 202. 48 1798 94. 69 119. 14 47. 77 336. 07 205. 61 16070 94. 60 96. 59 3. 46 128. 18 52. 11 23625 94. 57 138. 1348. 08319. 2091. 62 16775 94. 57 349. 58 178. 66 1164. 24 399. 53 21882 94. 51 486. 74 47. 85 758. 64 167. 24 24582 94. 45 69. 68 15. 24 31. 85 17. 38 14996 94. 42 206. 77 60. 78 471. 76 163. 11 24590 94. 36 43. 33 17. 37 166. 07 70. 63 4473 94. 36 67. 70 30. 48 172. 24 49. 29 8640 94. 33 66. 36 5. 36 141. 04 58. 77 23806 94. 33 167. 38 49. 48 459. 19 167. 23 21086 94. 21 164. 64 11. 89 103. 24 34. 93 21586 94. 18 70. 26 31. 01 220. 53 67. 79 2632 94. 09 197. 64 7. 08 154. 04 30. 64 21305 94. 06 194. 67 46. 54 437. 54 129. 56 18269 94. 00 394. 51 86. 48 771. 13 179. 69 5496 93. 96 268. 43 102. 39 651. 85 166. 35 Table 5D GLGC Identifier LDA Score Tox Group Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 14983 93.93 3935. 84 130. 20 5873. 51 4368. 56 729 93. 93 39. 48 6. 73 77. 25 26. 06 1929 93. 93 476. 55 93. 68 868. 90 216. 79 347 93. 87 123. 84 14. 40 78. 57 23. 09 3863 93. 87 25. 92 20. 32 196. 57 85. 56 20740 93. 84 355. 52 75. 34 210. 92 62. 22 17923 93. 81 83. 10 5. 93 58. 07 17. 69 15926 93.75 149. 75 18. 03 92. 20 42. 90 25692 93.75 70. 08 7. 62 156. 74 181. 44 4504 93. 75 445. 80 39. 02 1087. 15 323. 13 1159 93. 75 590. 14 150. 75 991. 96 225. 85 13939 93. 72 124. 71 48. 61 325. 12 109. 46 17469 93.72 34. 52 5. 63 72. 44 30. 50 17836 93. 69 121. 68 5. 52 90. 78 19. 92 22124 93. 60 116. 89 12. 88 78. 17 21. 00 20960 93.54 443. 32 50. 92 295. 69 74. 33 5497 93. 48 371. 29 150. 42 785. 01 190. 34 21672 93. 48 474. 43 83. 01 314. 66 77. 75 22669 93.45 61. 36 13. 28 33. 21 14. 07 15844 93. 36 70. 68 14.50 37.72 16. 43 20780 93.33 152. 07 119. 67 539. 74 202. 23 20809 93.33 437. 50 34.89 329.95 63. 72 21585 93. 18 157. 63 45. 39 342. 07 89. 26 13369 93.12 232. 19 7. 82 184. 45 38. 15 21123 93.09 321. 71 96. 61 661. 80 184. 33 15242 93. 06 108. 52 12. 92 80. 06 15. 30 1081 93. 03 278. 96 102. 51 527. 65 126. 56 4589 92. 97 724. 19 281. 99 1414. 61 338. 33 8664 92. 82 246. 38 136. 12 98. 44 245. 29 1877 92. 82 314. 31 125. 56 652. 38 170. 00 23699 92. 76 186. 00 34. 99 331. 03 104. 73 474 92. 73 490. 32 88.10 749.79 130. 85 1447 92. 70 268. 68 38. 24 201. 70 34. 81 8984 92. 67 399. 31 28. 86 308. 62 53. 47 Table 5E GLGC Identifier LDA Score Tox Group Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 17570 99. 82 642. 60 29. 35 240. 16 79. 04 25470 99. 79 125. 97 5. 72 31. 22 18. 52 19377 99. 76 215. 21 4. 72 109. 43 24. 18 455 99. 73 571. 19 126. 84 138. 41 189. 56 896 99. 67 191. 75 36. 71 23. 81 21. 26 9309 99. 67 329. 43 22. 61 174. 98 41. 72 17226 99. 64 253. 12 22.46 577.21 117. 15 699 99. 61 74. 54 12. 40 23. 01 34. 32 13563 99. 55 355. 81 42. 90 937. 62 228. 58 22540 99. 49 599. 57 49. 16 1780. 91 551. 74 23780 99. 43 120. 05 46. 77 20. 80 30. 16 17289 99. 43 410. 41 33. 11 1059. 53 278. 91 21959 99. 40 327. 36 32. 91 131. 72 41. 66 13973 99. 34 247. 62 42.45 33.40 20. 04 22984 99. 34 266. 02 27. 63 100. 26 30. 89 11421 99. 31 341. 72 20. 35 194. 63 40. 25 22618 99. 31 117. 66 20. 00 30. 61 11. 80 5497 99. 28 248. 05 17. 62 785. 70 189. 15 5929 99. 28 168. 33 15. 69 36. 89 20. 17 16007 99. 25 128. 45 19.80 21.47 13. 08 16610 99. 25 316. 65 10. 82 165. 32 65. 78 12606 99. 25 130. 99 7. 64 295. 10 99. 03 17695 99. 21 249. 77 34. 66 668. 20 180. 15 895 99. 21 668. 52 123. 70 177. 65 76. 45 23810 99. 21 84. 71 11. 03 27. 57 13. 19 3083 99. 21 158. 35 14. 18 74. 00 21. 63 16967 99. 18 136. 29 21. 82 33. 25 18. 18 17290 99. 18 509. 27 62. 67 1294. 21 373. 99 20494 99. 15 297. 13 78. 23 1055. 83 319. 86 894 99. 15 1783. 60 174. 73 652. 12 224. 42 16913 99. 15 613. 71 52. 52 1257. 86 287. 28 11079 99. 12 328. 58 20. 15 185. 07 44. 66 5206 99. 12 507. 97 41. 61 176. 59 77. 00 15273 99. 09 132. 66 22. 37 32. 60 18. 78 16726 99. 09 352. 81 48. 90 1059. 59 226. 33 17256 99. 09 125. 36 14. 47 429. 20 121. 73 19058 99. 06 122. 17 14. 88 52. 83 19. 42 17227 99. 06 499. 29 60. 99 982. 39 179. 08 1801 99. 06 255. 70 34. 95 89. 47 28. 47 23958 99. 06 203. 79 34. 98 61. 18 25. 94 23778 99. 03 364. 40 111. 41 62. 36 35. 91 20167 99. 03 96. 57 19. 35 24. 31 11. 29 3269 99. 03 366. 86 112. 74 81. 91 44. 65 3572 99. 03 172. 95 63. 76 38. 98 21. 80 16675 99. 00 328. 75 104. 16 29. 43 36. 26 7124 99. 00 529. 78 56. 03 1203. 74 312. 97 3925 99. 00 198. 37 20. 86 461. 33 112. 52 410 99. 00 465. 49 50. 55 1037. 75 225. 86 3584 99. 00 203. 98 20. 49 61. 56 30. 32 8325 98. 97 99. 90 20. 29 23. 02 13. 28 20828 98. 97 1005. 07 82. 88 323. 14 162. 23 2353398. 97 204. 49 10. 44 83. 11 38. 10 1993 98. 94 96. 08 5.11 24.14 17. 89 15008 98. 94 306. 66 36. 44 576. 58 114. 19 Table 5E GLGC Identifier LDA Score Tox Group Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 16676 98. 91 271. 51 96. 32 33. 53 29. 58 4450 98. 91 136. 12 13. 21 279. 34 61. 49 15437 98. 91 193. 06 63. 58 32. 08 19. 16 12616 98. 91 144. 41 20. 14 60. 76 20. 41 7665 98. 91 723. 79 74. 48 290. 61 94. 65 17301 98. 88 593. 47 75. 23 238. 07 75. 73 16674 98. 88 180. 45 57. 13 27. 50 22. 94 1564 98. 88 1294. 14 223. 87 44. 50 193. 91 16082 98. 88 129. 78 28. 85 40. 75 17. 41 23532 98. 88 124. 66 30. 17 22. 30 16. 51 1462 98. 85 1628. 61 155. 82 431. 68 216. 05 9084 98. 85 145. 53 46. 17 40. 68 17. 08 6022 98. 85 414. 10 35. 32 217. 84 63. 57 3099 98. 85 554. 56 35. 33 894. 32 163. 71 17535 98. 82 560. 61 73. 51 244. 84 64. 97 23699 98. 82 137. 82 16. 18 331. 30 104. 43 17514 98. 82 358. 61 50. 80 817. 29 188. 14 5952 98. 82 255. 47 23. 17 83. 50 40. 80 535 98. 79 96. 78 13. 35 38. 89 21. 47 21651 98. 79 211. 95 80. 37 26. 88 22. 79 5496 98. 79 219. 25 23. 70 652. 26 165. 76 15175 98. 79 116. 18 37. 93 319. 43 57. 36 23961 98. 79 379. 40 51. 33 785. 34 150. 80 18168 98. 79 168. 33 33. 83 38. 38 34. 80 16884 98. 79 1053. 19 76. 80 1909. 01 474. 48 25233 98. 76 62. 01 2. 18 31. 39 13. 04 19834 98. 76 416. 63 72. 40 169. 62 42. 80 21122 98. 76 534. 05 73. 79 1146. 33 236. 16 17661 98. 76 580. 72 105. 12 262. 94 68. 13 574 98. 73 912. 07 67. 77 352. 32 185. 51 1409 98. 73 201. 45 22. 59 438. 68 98. 73 20886 98. 70 94. 56 45. 86 798. 30 318. 63 8426 98. 67 120. 65 12. 99 49. 38 20. 34 1490 98. 67 52. 85 7. 86 20. 79 7. 83 17516 98. 64 304. 60 25. 38 547. 56 127. 91 16871 98. 64 206. 80 46. 25 79. 45 24. 72 22927 98. 64 210. 74 21. 37 84. 48 34. 52 7101 98. 61 3734. 58 971. 30 404. 36 664. 35 15790 98. 61 112. 29 21. 33 35. 96 18. 51 457 98. 61 897. 31 151. 83 285. 93 92. 35 1929 98. 61 362. 48 40. 32 869. 55 215. 82 16650 98. 58 650. 04 84. 16 256. 56 84. 67 15002 98. 55 420. 90 46. 06 135. 44 107. 26 17345 98. 55 263. 93 24. 68 127. 21 36. 29 20887 98. 52 191. 50 66. 84 871. 37 342. 61 16649 98. 52 361. 29 75. 07 105. 60 48. 12 7196 98. 52 549. 97 33. 63 177. 67 91. 15 1877 98. 52 254. 30 28. 09 652. 80 169. 49 20582 98. 52 287. 05 13. 73 487. 15 95. 43 Table 5F GLGC Identifier LDA Score Tox Group Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 23115 96. 27 218. 73 37. 94 504. 64 158. 87 18285 94. 66 425. 99 37. 64 688. 90 152. 65 18522 94. 29 477. 42 63.58 759.42 194. 18 21105 93. 53 188. 56 23.10 300.96 60. 90 9504 93. 05 71. 31 11.15 48.44 20. 69 13934 92. 71 180. 15 27. 02 68. 19 54. 80 11653 92. 35 269. 88 75. 12 561. 59 194. 36 15489 91. 68 96. 70 14. 21 141. 82 34. 76 3279 91. 44 394. 77 37. 63 552. 89 119. 12 2264 91. 41 134. 06 11. 12 101. 59 24. 28 2282 91. 08 90. 03 26. 05 212. 24 65. 58 22271 91. 08 114. 39 43. 35 247. 46 57. 55 11232 90. 98 413. 94 45. 20 291. 89 76. 35 11326 90. 95 191. 68 30.66 319.99 87. 52 1649 90. 83 363. 72 54. 17 561. 87 156. 83 10849 90. 74 108. 53 15. 45 73. 98 26. 10 11618 90. 72 179. 78 41. 87 381. 46 109. 96 13611 90.71 141. 12 35. 24 249. 73 83. 52 2912 90. 60 1472. 50 191. 19 2440. 94 597. 53 14978 90. 59 115. 74 17. 67 69. 00 30. 46 26133 90. 48 395. 06 106. 85 188. 25 84. 91 783 90. 47 122. 89 16. 37 83. 12 25. 36 11198 90. 47 66. 09 9. 13 43. 72 15. 80 13457 90. 47 108. 45 8. 39 75. 26 26. 79 4280 90. 44 2201. 62 242. 72 1538. 01 535. 02 17268 90. 32 317. 63 20. 88 445. 26 113. 01 25235 90. 29 187. 30 55. 17 84. 23 49. 84 5837 90. 29 586. 00 88. 17 850. 13 202. 51 165 90. 11 145. 31 43. 89 58. 63 36. 81 20555 90. 10 70. 09 13. 74 116. 38 35. 29 24233 90. 10 411. 31 46. 44 567. 75 108. 66 26173 90. 08 265. 60 25. 65 171. 81 48. 30 9332 90. 02 39. 70 10. 71 102. 53 42. 52 4451 90. 01 192. 78 31. 81 290. 75 72. 79 5430 89. 98 60. 14 21. 49 135. 42 58. 52 16887 89. 89 107. 51 10. 43 154. 97 45. 52 4987 89. 86 161. 07 15. 62 234. 26 58. 10 15904 89. 80 81. 53 10. 99 56. 69 23. 58 22985 89. 78 61. 31 12. 25 109. 17 29. 50 2964 89. 74 207. 16 29. 50 295. 32 59. 24 150 89. 74 44. 55 4. 99 31. 82 9. 68 12684 89. 68 216. 15 19. 77 153. 61 44. 73 1946 89. 66 64. 08 9. 55 39. 55 12. 41 10069 89. 56 267. 84 30. 41 197. 01 47. 53 18447 89. 54 602. 70 133. 92 1098. 88 276. 35 19930 89. 51 49. 33 6. 03 28. 71 11. 78 13020 89. 44 111. 03 18. 18 74. 64 23. 70 14410 89. 40 133. 78 15. 12 184. 02 38. 17 22929 89. 40 330. 05 142. 49 797. 70 312. 82 19890 89. 34 114. 05 11.07 80.22 26. 45 15028 89. 26 172. 40 66. 68 366. 39 126. 77 6630 89. 22 1020. 91 101. 07 1270. 63 199. 90 894489. 19 61. 509. 2240. 4516. 66 23748 89. 13 67. 98 29. 82 154. 15 63. 22 Table 5F GLGC Identifier LDA Score Tox Group Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 15039 89. 11 118. 00 47. 79 272. 70 91. 84 20149 89. 08 2751. 06 487. 03 1546. 67 703. 21 21400 89. 05 217. 92 45. 44 361. 83 72. 95 7825 89. 05 120. 48 23. 58 70. 06 27. 39 12945 89. 02 168. 30 33. 30 289. 09 69. 55 1644 88. 98 444. 20 28. 05 560. 84 126. 28 16087 88. 96 147. 89 19. 38 87. 68 30. 47 11075 88. 93 99. 43 19. 68 58. 88 21. 11 19943 88. 92 210. 88 54. 72 366. 97 116. 34 21147 88. 84 223. 85 45. 68 361. 29 80. 82 3407 88. 84 48. 51 16. 65 22. 82 14. 74 12366 88. 81 402. 17 110. 21 266. 10 83. 20 17833 88. 80 178. 08 13. 51 132. 77 41. 58 11968 88. 75 161. 58 45. 48 277. 70 74. 95 6886 88. 66 74. 86 18. 86 44. 24 15. 63 5531 88. 65 41. 41 2. 58 32. 86 11. 29 11866 88. 65 193. 70 21. 24 133. 49 72. 18 17363 88. 40 836. 27 72.73 1036.86 193. 05 21253 88. 40 346. 51 35. 62 476. 31 102. 82 2574 110. 78 17. 74 72. 92 19. 69 2439 88. 38 98. 92 17. 04 147. 82 27. 80 9035 88. 25 93. 11 9. 82 126. 24 27. 10 291 88. 11 145. 69 31. 30 224. 02 46. 48 24165 88. 10 119. 54'5. 30 72. 25 33. 85 10071 87. 87 177. 18 42. 47 350. 75 123. 95 187 87. 75 202. 63 72. 64 75. 52 52. 59 28 87. 68 260. 01111. 55531. 88180. 16 17921 87. 55 119. 45 22. 88 195. 17 71. 34 24567 87. 37 34. 58 19. 86 111. 01 63. 84 20617 86. 99 425. 33 118. 93 206. 81 228. 40 22386 86. 89 148. 02 26. 48 252. 07 98. 25 8829 86. 69 454. 94 86. 93 283. 22 86. 03 25921 86. 50 50. 94 6. 86 28. 33 16. 05 25364 86. 35 104. 43 36. 32 56. 18 57. 10 8599 86. 17 222. 32 55. 03 389. 47 116. 57 17357 85. 93 89. 91 76. 51 270. 04 95. 73 20582 85. 77 353. 36 43. 17 487. 57 95. 61 20896 85. 56 83. 44 18. 33 141. 36 40. 26 1535 85. 53 44. 01 11. 60 85. 58 31. 50 15303 85.43 68.69 852 95.79 28.70 18716 85.36 53.32 13.29 29.64 11.72 25662 85. 35 210. 06 62. 21 117. 83 97. 01 24438 85. 26 89. 77 17. 89 143. 35 40. 49 6577 85. 16 122. 77 12. 31 178. 46 48. 88 21193 84. 95 50. 26 5.87 33.25 14. 85 1409 84. 89 299. 53 60. 23 438. 92 99. 13 15330 84. 84 36. 66 19. 02 81. 96 24. 24 15191 84. 83 3728. 02 829. 67 2407. 15 1233. 18 6049 84. 79 805. 83 63. 05 688. 66 113. 01 18043 84. 79 99. 39 38. 52 41. 39 22. 49 24431 84. 79 131. 55 52. 25 59. 17 87. 36 3870 84. 58 91. 07 23. 43 152. 03 56. 60 22219 84. 55 61. 9415. 6037. 4862. 65 15642 84. 42 750. 42 224. 71 433. 34 115. 91 Table 5F GLGC Identifier LDA Score Tox Group Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 24631 84, 37 36. 22 7. 30 21. 68 10. 08 19003 84. 31 141. 69 17. 27 102. 43 33. 94 25777 84. 09 809. 02 317. 73 441. 84 253. 01 23000 84. 06 41. 94 3. 47 35. 87 9. 55 2079 84. 04 190. 93 36. 44 304. 09 90. 50 439 84. 00 28. 56 7. 59 45. 33 16. 65 8426 83. 89 77. 60 12. 47 49. 42 20. 66 16205 83. 86 1418. 72 140. 70 1122. 95 425. 85 5838 83. 75 443. 80 68. 13 652. 08 145. 88 3609 83. 65 185. 56 111. 40 434. 86 172. 76 989 83. 64 106. 37 20.93 147.41 60. 77 4373 83. 62 166. 60 16. 69 133. 42 26. 68 22562 83. 52 46. 00 10. 04 27. 10 13. 28 22783 83. 50 566. 84 84. 58 347. 17 212. 46 16227 83. 44 152. 60 38. 37 88. 54 40. 73 25399 83. 38 392. 81 122. 41 185. 18 190. 17 2191 83 : 36 42. 32 13.37 22.22 8.81 3512 83. 28 129. 79 11. 72 106. 87 19. 31 22434 83. 07 68. 42 18. 29 43. 74 20. 91 3465 82. 92 173. 23 36. 47 263. 26 79. 05 18246 82. 90 113. 80 43. 37 258. 83 95. 85 16116 82. 88 61. 16 6. 60 78. 82 19. 59 25589 82. 84 220. 29 33. 93 150. 66 41. 90 1529 82. 83 226. 95 35. 67 294. 63 70. 00 22781 82. 81 229. 37 43. 64 143. 62 72. 36 13974 82. 76 355. 79 36. 94 315. 24 173. 81 13610 82. 68 257. 86 38. 84 365. 13 107. 29 23781 82. 57 67. 71 7. 21 85. 97 27. 49 25647 82. 56 437. 20 166. 12 209. 40 238. 75 24566 82. 52 103. 57 24. 04 179. 92 89. 90 25686 82. 52 899. 95 98. 60 749. 37 152. 25 1453 82. 50 89. 33 27. 93 52. 20 26. 79 Table 5G GLGC Identifier DA Score Tox Grou Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 472 99. 03 243. 72 82. 34 732. 71 178. 26 22675 98. 67 118. 93 55.69 28.15 15. 37 574 98. 51 1391. 19 255.85 347.01 165. 41 1564 98. 51 924. 30 353. 42 42. 69 192. 73 15003 98. 33 454. 25 157. 22 31. 60 90. 05 15004 98. 30 770. 01 324. 95 154. 94 147. 16 646 98. 30 83. 09 64.74 528.44 191. 02 15002 98. 27 571. 32 171. 32 133. 34 101. 38 22592 98. 27 1074. 58 313. 00 224. 39 160. 59 10015 98. 18 563. 53 77. 79 229. 49 80. 02 10983 98. 15 26. 59 14. 05 150. 11 58. 58 20816 98. 12 1222. 71 372.23 405.88 177.08 14929 98. 12 2704. 92 750.05 750.97 385. 07 17325 98. 06 566. 28 234. 26 55. 28 99. 39 25702 97. 97 1078. 58 151. 22 623. 33 125. 71 16350 97.91 140.55 45.36 43.66 26. 40 603'997. 88 656. 26 129.35 309.49 76. 09 645 97. 85 22. 16 19. 08 135. 98 49. 42 10109 97. 82 1679. 00 1324. 10 1190. 54 238. 15 10016 97.79 518. 59 107. 36 208. 97 79. 42 21797 97. 79 751. 43 151. 51 331. 28 105. 33 20885 97. 75 86. 92 67. 69 590. 89 224. 65 18751 97. 72 1011. 52 204. 86 514. 43 129. 28 18503 97. 69 87. 10 55. 82 769. 37 319. 53 10839 97. 69 522. 43 88. 99 296. 05 56. 93 4327 97. 66 213. 79 52.87 82.05 36. 57 24211 97. 63 363. 77 83.59 128.82 74. 63 1551 97. 57 44. 36 13. 06 122. 96 105. 41 20848 97. 57 1070. 75 145.58 548.58 158.87 22321 97. 54 321. 53 86. 82 93. 58 65. 67 11205 97. 54 218. 47 59.26555.88 160. 64 23651 97. 51 3310. 38 741.12 733.68 659.72 20481 97. 51 104. 65 12.92 201.59 40. 93 4856 97. 51 225. 36 26. 28 113. 64 35. 44 14677 97. 45 165.57 17.88 69.76 30.34 15876 97. 45 2120. 60 249.97 1361.28 237. 57 15132 97. 42 556. 28 65. 10 314. 76 79. 74 16245 97. 42 69. 92 89.96 412.35 124. 91 19188 97. 42 527. 70 117. 58 1311. 37 331. 19 20884 97. 39 71. 11 94.30 738.14 289. 89 1422 97. 39 102.77 18.65 300.99 104. 53 5838 97. 36 301. 27 68. 21 652. 99 143. 93 15955 97. 18 283. 29 93. 14 689. 98 159. 09 7307 97. 18 92. 05 30.06 28.29 16.83 21509 97. 18 356. 98 61.72 91.05 94. 62 736 97. 15 1042. 03 152. 24 635. 04 130. 62 17357 97. 12 50. 26 40. 35 270. 21 95. 37 15662 97. 06 163.93 19.51 93.95 27. 11 13646 97. 06 1401. 63 217.84 815.38 181.16 17807 97. 06 1436. 26 188.44 842.88 218. 96 19679 97. 03 257. 82 106. 61 757. 15 199. 62 23961 97. 00 451. 82 79.40 786.13 150.14 16204 96. 97 1384.43 194.54 865.08 172. 51 18750 196. 91 341. 14 53. 21 168. 24 62. 25 Table 5G GLGC Identifier LDA Score Tox Group Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 5208 96. 88 256. 89 147. 95 977. 27 392. 75 25419 96. 81 31. 08 22. 07 149. 42 67. 18 7964 96. 81 121. 19 45. 58 325. 72 93. 20 19824 96. 75 72. 58 25. 39 216. 05 72. 84 3834 96. 75 132. 71 15.15 223.31 50. 13 16929 96. 69 1743. 43 228.03 1095.03 207. 82 11849 96. 69 1317. 16 211. 89 773. 90 177. 28 18612 96. 69 212. 66 25. 56 28. 14 27. 31 1141 96. 60 436. 63 69.87 241.00 65. 86 17514 96. 57 454. 63 81. 01 818. 94 186. 75 4441 96. 54 1550. 03 172.22 1061.96 187. 57 25802 96. 54 845. 70 105. 36 521. 07 117. 59 12332 96. 54 184. 06 71.27 549.08 160. 38 24108 96. 54 257. 44 35. 85 149. 90 36. 24 1382 96. 51 90. 08 11.91 49.24 15. 74 4360 96. 45 162. 70 43. 83 333. 15 72. 47 4445 96. 39 803. 11 134. 14 477. 79 96. 26 25415 96. 36 32. 48 27. 25 161. 84 72. 36 17284 96. 30 121. 14 16. 57 218. 48 58. 98 2125 96. 27 190. 48 54. 94 69. 66 70. 52 6614 96.21 183.60 64.33 438.27 117. 69 17361 96. 18 28. 93 11.40 138.07 55. 62 13647 96. 15 1685. 74 240. 33 965. 67 279. 68 3121 96. 09 495. 24 184. 53 1291. 00 320. 21 23093 96. 03 106. 37 12. 36 186. 37 43. 33 20873 96. 03 3443. 13 613.84 2121.19 488. 68 15135 96. 00 1256. 66 187. 64 774. 12 176. 10 6405 95. 90 202. 88 43. 49 403. 99 105. 10 968 95. 78 29. 31 9.99 81.27 22. 89 19943 95. 78 148. 72 40. 47 367. 33 115. 68 5199 95. 57 231. 08 78.06 560.22 167. 42 16150 95. 51 274. 61 48. 72 520. 97 135. 92 23758 95. 45 88. 49 20. 75 175. 01 41. 28 21078 95. 42 318. 58 74. 48 629. 47 142. 80 28 95. 42 145. 06 98. 13 532. 55 178. 76 2465 95. 39 67. 67 23. 37 131. 86 26. 71 1508 95. 33 269. 31 91. 76 654. 52 194. 51 3610 95. 33 430. 67 215. 13 1122. 89 327. 90 18629 95. 30 1002. 30 147.79 653.52 144. 64 3069 95. 27 95. 79 24.02 181.96 42. 00 25467 95. 21 320. 12 106. 53 737. 06 245. 44 20810 94. 99 2328. 92 400.59 1448.17 356. 77 4449 94. 72 115. 32 31. 26 243. 54 69. 77 15653 94. 60 1852. 53 268. 29 1284. 72 282. 04 24770 94. 57 60. 89 37. 80 244. 14 106. 68 20716 94. 54 407. 31 96. 00 723. 45 165. 86 1549 94. 54 114. 38 21. 37 201. 87 48. 01 21950 94. 42 493. 04 82. 54 812. 67 152. 27 1546 94. 36 122. 71 35.02 244.53 64. 28 24564 94. 35 97. 01 57. 45 615. 45 190. 61 24563 94. 16 24. 77 36. 61 322. 32 110. 47 457 94. 10 658. 43 132. 04 285. 53 94. 14 17198 94. 10 174. 10 183.51 910.03 269. 39 18502 93.98 124. 08 73.30 765.24 269. 62 Table 5G GLGC Identifier LDA Score Tox Group Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 21695 93. 92 142. 04 27. 58 49. 80 30. 26 16351 93. 86 224. 63 88. 04 65. 23 32. 31 3870 93. 84 56. 07 22. 14 152. 24 56. 26 199393. 77 93. 20 19. 75 23. 92 17. 40 19040 93. 71 706. 16 170. 63 181. 75 113. 25 7196 93. 65 574. 19 128. 31 176. 23 87. 09 1501 93. 65 224. 82 95. 99 51. 78 53. 84 20886 93. 62 80. 08 149. 92 801. 44 315. 41 20849 93. 47 566. 69 140. 91 281. 36 87. 91 1809 93. 44 275. 58 89. 54 34. 04 133. 49 1463 93. 38 1519. 27 270. 01 664. 00 313. 79 7489 93. 33 22. 54 9.10 72.97 31. 20 18453 93. 28 88. 03 19. 21 218. 34 72. 82 16726 93. 28 486. 85 132 99 1061. 35 225. 30 20887 93. 22 168. 32 177. 62 874. 64 339. 69 2109 93. 19 1476. 03 210. 52 911. 33 166. 60 1462 93. 19 954. 56 196. 88 432. 34 223. 37 25718 93. 13 683. 37 89. 19 419. 94 86. 09 17159 93. 07 1527. 58 315. 26 787. 22 213. 24 17104 93. 04 855. 38 133. 20 481. 52 111. 05 17401 93. 04 2406. 67 718. 29 1005. 70 409. 58 23854 93. 04 1043. 25 158. 05 521. 42 171. 16 3430 92. 98 1105. 90 415. 94 451. 02 154. 70 19768 92. 92 1379. 96 280. 91 786. 38 167. 89 25691 92. 89 1341. 48 251. 62 775. 97 169. 40 7197 92. 89 474. 21 129. 15 188. 31 86. 11 Table 5H GLGC Identifier LDA Score Tox Group Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 1698 95. 69 476. 04 217. 52 66. 29 80. 81 19254 93. 32 450. 27 111. 28 243. 51 70. 21 23917 92. 66 1506. 66 499. 29 718. 95 184. 83 17541 92. 42 1949. 27 848. 82 715. 92 315. 92 20803 91. 23 799. 85 172. 29 470. 96 121. 12 1537 90. 76 257. 23 167.48 25. 97 54. 59 25069 90.61 345. 14 130. 65 122. 58 64. 89 18990 90. 28 86. 48 40.00 20.60 20. 74 20795 89. 27 395. 60 169. 67 145. 49 73. 47 6014 89. 18 250. 89 107. 92 79. 07 39. 75 13609 89. 08 127. 39 51. 22 239. 16 63. 31 353 88. 14 319. 61 99. 94 169. 89 88. 77 19252 88. 05 1076. 93 223.42 699.29 132.43 1399 87. 58 525. 84 225. 50 194. 83 76. 18 20802 87. 50 435. 04 93. 17 244. 10 82. 49 20804 87. 44 1875. 82 427. 00 1059. 53 324. 98 24192 87. 16 197. 41 91. 63 74. 59 46. 05 2059 87. 00 193. 67 24. 25 136. 36 35. 16 11755 86. 73 376. 55 164. 92 141. 89 130. 13 14970 86. 63 129. 6833. 81200. 0440. 68 21038 86. 52 242. 02 70. 96 103. 82 41. 91 21039 86. 46 195. 33 59. 92 78. 33 43. 60 22352 86.44 284. 98 97. 78 147. 56 105. 44 4944 86. 29 211. 24 47. 96 119. 87 58. 35 2242 86. 21 1439. 71 469. 38 2188. 97 546. 30 20035 86. 06 430. 87 178. 90 180. 79 99. 78 14347 85.85 400. 13 169. 40 165. 49 124. 98 14633 85. 60 234. 78 89. 03 88. 80 83. 21 15964 85. 54 674. 79 216. 85 1091. 41 285. 42 12812 85. 49 52. 00 16. 73 97. 11 34. 86 22502 85. 39 158. 92 82.43 53.23 48. 19 11840 85. 36 122. 01 37. 49 67. 99 20. 17 354 85. 33 388. 15 110. 75 216. 19 104. 30 23314 85. 33 562. 77 365. 79 72. 82 278. 18 13610 85. 29 239. 35 63.10 365.74 106.91 3816 85. 24 464. 69 118. 27 309. 23 67. 90 15171 84. 95 419. 71 164.49 224. 19 79. 03 22501 84. 65 492. 96 180. 94 251. 35 55. 90 8820 84. 40 597. 48 343. 99 137. 31 114. 55 5863 84. 29 88. 93 23. 67 139. 47 34. 68 24235 84. 25 1152. 14 527. 92 473.62 203. 30 405 83. 80 132. 67 34. 34 208. 32 63. 52 12331 83. 65 391. 83 107. 95 591. 12 141. 29 1410 83. 60 34. 40 19. 24 89. 22 43. 41 22197 83. 56 181. 41 38. 36 111. 12 43. 86 17892 83. 55 153. 95 40. 92 306. 40 134. 74 21513 83. 49 75. 92 24. 74 120. 24 29. 73 11429 83. 43 212. 12 34. 36 269. 26 41. 65 20895 83. 42 188. 70 90. 22 303. 22 74. 58 12848 83. 34 297. 78 63.29 431.68 92. 39 18259 83. 24 519. 34 278. 97 208. 74 145. 33 3822 83. 20 1346. 58 265. 08 925. 26 284. 34 24246 83. 14 450. 51 118.31 305.90 95. 78 2632 83. 14 122. 74 47. 18 31. 65 49. 47 Table 5H GLGC Identifier LDA Score Tox Group Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 18396 83. 12 111. 98 44. 34 66. 03 26. 28 3053 83. 04 154. 60 38. 76 96. 88 33. 21 16718 83.02 771. 65 152. 36 1131. 02 291. 60 12979 82.91 827. 72 363. 04 363. 63 189. 87 26319 82. 82 76. 87 13. 91 48. 99 22. 63 352 82. 73 127. 68 32. 93 81. 40 54. 77 17850 82. 65 478. 49 74.33 350.42 68. 02 16726 82. 61 775. 42 171. 63 1060. 46 228. 56 25902 82. 59 112. 19 22. 14 159. 55 48. 13 6765 82. 55 507. 81 142. 81 730. 21 168. 95 22625 82. 55 203. 73 89. 37 109. 20 101. 37 20086 82. 52 270. 19 119.18 107.78 72.84 22414 82. 49 91. 38 20. 25 62. 37 32. 42 15069 82. 45 156. 30 69. 08 89. 93 53. 08 23435 82.42 143. 51 70.04 32.23 45. 61 13607 82. 37 34. 94 7. 53 22. 53 9. 86 15382 82. 29 978. 24 634. 06 120. 29 179. 44 22656 82. 26 199. 64 38. 98 123. 05 53. 17 26083 82. 21 1826. 66 491. 08 1187. 90 721. 09 19184 82. 21 185. 49 78. 89 78. 67 75. 04 13611 82. 20 130. 10 78. 13 250. 25 82. 89 16039 82. 15 697. 44 191. 99 482. 12 97. 81 2924 82. 14 213. 38 38. 03 154. 90 50. 18 8283 82. 11 273. 51 122. 40 128. 67 44. 94 4235 82. 01 583. 10 107. 05 411. 30 95. 75 22413 81. 99 109. 06 23.31 68.44 38.34 3091 81. 96 479. 65 112. 26 714. 58 157. 74 1651 81. 95 628. 76 65. 78 789. 11 181. 29 8211 81. 93 3918. 21 2663. 36 3502. 10 1459. 77 20841 81. 92 143. 31 33. 78 95. 74 25. 14 12978 81. 88 178. 61 68. 70 96. 11 47. 83 13349 81. 88 200. 63 47. 75 132. 83 38. 04 20082 81. 87 91. 12 20. 35 66. 30 28. 33 1439 81. 65 147. 91 28. 34 225. 64 53. 27 14346 81. 56 203. 45 102. 23 50. 68 82. 80 15470 81. 55 446. 71 86. 23 334. 66 93. 68 15295 81. 48 211. 13 62. 16 133. 01 44. 12 20443 81. 46 161. 56 35. 20 113. 93 27. 53 2979 81. 44 245. 69 57. 16 282. 97 42. 84 24033 81. 42 259. 06 80. 18 347. 59 75. 37 1558 31.39 321.49 76.64 200.81 63. 40 24377 81. 36 145. 34 38. 16 203. 71 49. 55 15296 81. 36 211. 59 76. 79 126. 72 51. 34 15032 81. 33 183. 52 59. 26 265. 32 74. 21 19433 81. 22 249. 89 135. 26 95. 01 61.36 4956 81. 16 164. 38 98. 90 69. 29 29. 02 18011 80. 90 67. 94 34. 59 27. 48 28. 90 4592 80. 90 249. 94 54. 72 177. 09 36. 45 25253 80. 87 356. 00 58. 62 290. 00 68. 77 18449 80. 81 729. 28 116. 57 610. 20 123. 99 17736 80. 81 182. 31 146. 86 69. 27 157. 44 20801 80. 66 227. 27 55. 54 150. 06 48. 38 22412 80. 58 140. 47 30. 74 91. 22 45. 78 18597 80. 46 1089. 16 347. 96 559. 47 193. 08 Table 5H GLGC Identifier LDA Score Tox Group Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 21239 80.43 229. 76 97. 82 106. 28 59. 82 15574 80. 39 173. 01 25. 25 215. 63 33. 89 18967 80.39 337. 68 55. 22 487. 47 203. 79 3016 80. 37 4148. 89 2854. 50 3998. 79 1813. 37 21305 80. 36 272. 12 81. 64 438. 75 129. 17 24484 80. 31 66. 39 12. 02 92. 42 26. 08 25064 80. 28 2074. 70 700. 66 1115. 73 310. 65 4392 80. 03 3259. 52 1607. 18 2948. 56 850. 63 18300 79.97 206. 84 132. 88 487. 38 169. 27 24900 79. 96 488. 04 143. 15 638. 38 155. 04 25098 79.90 93. 64 67. 91 36. 16 34. 64 21147 79. 81 268. 70 99. 55 361. 28 80. 70 15750 79.71 47. 36 18. 14 21. 51 14. 89 Table 51 GLGC Identifier LDA Score Tox Group Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 2242 82. 51 1386. 39 557. 25 2237. 29 505. 01 5601 80. 41 570. 05 236. 57 903. 71 216. 83 4944 80. 39 210. 32 80.95 114.51 51. 54 15032 78. 99 176. 05 67. 41 270. 72 70. 95 13610 78. 86 260. 43 88. 06 371. 73 104. 73 3610 78. 84 722. 35 368. 53 1146. 23 311. 02 5863 78. 76 96. 37 30. 11 141. 94 33. 29 1529 78. 54 203. 36 69. 83 300. 60 65. 42 17682 78. 29 507. 13 211. 81 773. 82 172. 62 10985 78. 22 735. 68 231. 86 1069. 30 225.65 21632 77. 91 98. 75 74. 15 27. 96 44. 65 28 77. 64 315. 43 178. 66 545. 11 171. 54 15964 77. 61 745. 68 276. 40 1111. 07 273. 12 17550 77. 50 879. 01 298.17 1290.95 333. 72 23314 77. 31 506. 68 414. 87 47. 74 245. 21 17524 77. 19 794. 19 308. 69 1135. 59 259. 89 11618 77. 12 257. 75 117. 01 388. 64 105. 31 23435 77. 07 107. 07 69.42 28.24 40. 65 812 76. 93 105. 28 36. 08 153. 16 36. 80 13609 76. 92 163. 7755. 10243. 1961. 57 3091 76. 77 535. 18 168. 51 724. 55 150. 86 16312 76. 70 108. 77 62. 22 45. 54 31. 63 20694 76. 61 688. 47 220. 38 933. 57 204. 17 19679 76. 55 499. 67 216. 56 771. 74 190. 03 14970 76. 36 144. 83 50. 08 203. 14 37. 69 24496 76. 32 72. 15 40. 14 113. 67 35. 59 10818 76. 28 251. 30 167. 92 480. 32 177. 62 18337 76. 16 1120. 66 375. 56 1593. 01 326. 83 1698 76. 15 259. 77 253.73 57. 45 46. 82 2702 76. 15 433. 75 181. 46 270. 79 68. 25 17755 76.09 278. 24 99. 73 390. 16 92. 04 7489 75. 92 37. 03 20. 90 75. 16 30. 46 21654 75. 86 551. 82 178. 12 366. 37 116. 43 15299 75. 82 120. 11 57. 11 72. 50 54. 88 13349 75. 79 183. 06 52. 76 130. 07 35. 07 1159 75. 77 712. 96 239. 20 1011. 11 211. 67 18272 75. 77 134. 16 52. 28 179. 70 40. 85 23005 75. 72 694. 34 270. 62 901. 12 190. 44 8721 75. 64 109. 17 63. 60 188. 60 63. 43 10887 75. 63 42. 57 19. 85 65. 79 22. 04 3916 75. 59 472. 89 195. 40 675. 96 140. 94 16314 75. 54 110. 20 71. 12 41. 23 39. 76 22554 75. 51 387. 64 139. 23 544. 84 133. 65 5384 75. 41 90. 12 61. 25 28. 04 36. 31 7936 75. 30 107. 61 27. 73 139. 51 30. 80 5923 75. 17 439. 81 176. 29 606. 68 131. 73 19184 75. 15 190. 82 119. 94 71. 94 64. 87 21239 75. 09 197. 82 98.17 101.23 52.71 3874 74. 97 637. 40 187. 18 871. 96 181. 31 5900 74. 94 205. 87 72. 79 265. 10 54. 52 7784 74. 81 532. 12 161. 80 699. 90 128. 21 18522 74.81 548. 81 212. 63 772. 15 185. 03 22569 74. 81 417. 82 171. 09 628. 93 157. 19 2555 74. 79 134. 28 53. 66 81. 97 40. 03 Table 51 GLGC Identifier LDA Score Tox Group Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 9673 74. 72 35. 38 16. 35 65. 52 2 4473 74. 68 122. 22 55. 23 175. 55 47. 15 23917 74. 67 1098. 72 458. 70 701. 40 145. 27 20458 74. 64 271. 25 94. 25 374 56 94. 29 6674 74. 54 1776. 75 507.96 2387.57 539.31 4360 74. 46 253. 43 81. 01 337. 54 69. 89 3995 74. 45 447. 64 135. 49 615. 34 139.51 6046 74. 40 135. 01 56. 88 197. 57 60. 74 11164 74. 38 332. 33 139. 83 485. 92 129. 73 9079 74. 38 581. 21 173. 48 749. 66 159. 41 15955 74. 37 490. 57 195. 79 701. 12 150. 24 22612 74. 35 330. 37 111. 38 469. 08 108. 90 6765 74. 29 544. 27 202. 38 740. 81 159. 94 21147 74. 26 274. 00 87. 67 366. 40 77. 47 4291 74. 22 180. 51 91. 51 288. 32 84. 88 4463 74. 19 86. 69 63. 34 154, 87 56. 17 4462 74. 15 658. 57 311. 71 971. 30 305. 73 9781 74. 13 82. 19 36. 96 124. 27 34. 07 14095 74. 13 270. 72 76. 14 358. 04 71. 36 13618 74. 08 137. 35 40. 63 99. 14 26. 21 18271 74. 07 587. 16 201. 63 753. 02 149.78 22681 74. 06 507. 76 361.88 202.52 156. 32 21157 74. 05 549. 82 137. 16 428. 96 84. 27 23261 74. 04 1121. 37 378. 88 1550. 48 320. 61 2370 74. 04 876. 31 227. 54 1077. 70 174. 57 10130 74. 03 167. 62 59. 58 224. 47 53. 57 11937 74. 01 101. 08 23.16 79.06 19.14 811 73.98 180. 08 66. 32 257. 46 56. 05 12979 73. 96 632. 88 317. 40 350. 02 172. 71 23546 73. 90 549. 94 189. 79 721. 45 151. 51 20801 73. 86 215. 55 69. 25 146. 31 43. 89 409 73. 83 746. 67 188. 60 947. 21 178. 98 4440 73. 83 195. 43 69. 44 295. 13 82. 26 21305 73. 82 298. 39 90. 29 446. 76 126. 64 22101 73. 80 85. 02 82. 10 175. 65 80. 50 15330 73. 67 58. 68 23. 74 83. 24 23. 75 20161 73. 64 80. 23 54. 25 29. 99 27. 33 15050 73. 63 541. 66 141. 16 688. 65 174. 84 16813 73. 61 231. 75 81. 80 331. 59 80. 11 18792 73. 60 98.71 33.22 136.87 36. 34 16756 73. 57 240. 33 81. 11 168. 05 37. 88 21341 73. 57 463. 05 136. 52 620. 74 147. 68 3467 73. 54 461. 68 163. 07 646. 99 168. 60 20082 73. 54 102. 09 38. 64 64. 04 25. 68 15039 73. 52 177. 90 93.67 278.20 88. 82 9905 73. 49 576. 55 180. 69 755.53 145. 11 15986 73. 46 214. 52 95.30 326.69 83.60 9053 73. 45 190. 10 53.40 240.11 47. 80 1460 73. 32 302. 66 131. 64 185. 02 73. 88 15111 73. 26 785. 18 294.19 1118.72 264. 03 15110 73. 25 505. 21 179. 79 713. 50 178. 30 15112 73. 00 1338. 19 433. 49 1860. 86 460. 35 354 72. 87 373. 67 185.53 207.02 87.88 25198 72. 83 49. 29 21.40 25.88 13. 23 Table 51 GLGC Identifier LDA Score Tox Group Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 21683 72. 77 53. 28 30. 07 25. 72 19. 21 16726 72. 69 800. 41 280. 17 1075. 60 214. 53 18300 72. 65 285. 09 167. 97 498. 43 162. 68 353 72. 64 298. 13 157. 91 162. 53 75. 73 4198 72. 64 603. 75 177. 10 780. 82 177. 13 24234 72. 61 391. 71 269. 60 175. 87 68. 56 6641 72. 55 304. 37 93. 60 402. 49 84. 73 15296 72. 54 195. 64 91.33 122.82 44. 73 23783 72. 45 376. 37 89. 08 460. 99 76. 97 4327 72. 45 133. 62 67. 44 79. 38 32. 50 18128 72. 27 163. 39 43. 26 205. 45 45. 93 18000 72. 20 1021. 88 441. 49 1515. 83 541. 89 10464 72. 19 90. 84 30. 16 122. 79 30. 91 24235 72. 19 833. 55 457. 25 456. 15 168. 02 1399 72. 16 341. 24 183. 76 188. 40 64. 08 18396 72. 13 106. 40 55.73 63.70 20. 92 20753 72. 02 157. 80 39. 75 117. 80 25. 81 25567 71. 99 715. 87 268.63 465.90 181. 93 17256 71. 98 313. 90 166. 05 436. 12 114. 73 14121 71. 92 492. 14 155. 94 350. 47 102. 93 16012 71. 84 101. 22 49. 06 62. 06 26. 39 11840 71. 83 96. 37 36. 59 66. 61 18. 13 17684 71. 81 170. 05 66. 05 237. 48 55. 17 15701 71. 80 47. 52 19. 49 30. 00 11. 38 794 71. 77 143. 65 62. 53 212. 58 63. 38 24770 71. 76 149. 41 95. 43 249. 51 105. 16 11483 71. 74 141. 85 116. 98 51. 93 39. 61 15295 71. 74 190. 57 76. 92 129. 84 38. 91 3430 71. 70 651. 98 230. 79 441. 70 152. 47 20056 71. 66 246. 08 95. 02 318. 69 67. 21 12031 71. 64 192. 48 67. 66 134. 78 33. 69 23961 71. 60 644. 10 203. 09 793. 72 143. 04 20803 71. 57 629.95 256. 03 463. 60 103. 39 17541 71. 55 1248. 41 894. 94 692. 89 234. 54 12978 71. 54 152. 96 71. 09 93. 05 44. 29 17734 71. 52 279. 85 275. 77 104. 11 64. 03 18360 71. 37 154. 88 51. 56 206. 67 54. 97 17196 71. 36 99. 85 27. 32 128. 69 24. 41 17301 71. 34 325. 89 119.33 233.24 70. 86 25777 71. 29 882. 80 556. 03 413. 32 182. 36 20298 71. 28 409. 64 131. 62 556. 86 153. 30 16775 71. 26 800. 69 398. 31 1188. 38 388. 39 17357 71. 23 178. 34 104. 23 275. 09 93. 07 18906 71. 16 164. 62 90. 59 266. 79 88. 78 1884 71.12 208.69 48.64 169.12 34.33 Table 5J GLGC Identifier LDA Score Tox Group Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 17829 92. 65 759. 68 633. 86 2726. 68 1360. 50 25468 90.11 657. 58 614. 46 2655. 18 1078. 33 24109 89. 60 75. 68 42. 47 221. 62 99. 80 1684 89. 47 788. 73 736. 74 3493. 87 1629. 14 25469 89. 11 523. 47 471. 39 1875. 13 750. 57 1688 88. 99 985. 99 996. 97 5062. 79 2851. 87 20082 86. 48 84. 34 9. 94 66. 36 28. 45 4312 85. 90 125. 63 20. 84 65. 92 30. 34 14003 85. 48 588. 35 140. 53 940. 91 244. 68 5129 85. 32 88. 98 34.42 179.18 56. 59 1685 85. 14 1891. 26 1942. 12 8508. 70 4812. 11 7489 84. 90 26. 53 14.62 73.20 31.11 1687 84. 65 544. 45 532.83 1797. 73 696. 06 494 84. 50 1183. 13 183.42 774.08 266.75 17743 84. 44 74. 48 35. 97 103. 03 28. 16 20864 84. 41 1168. 66 229. 66 1938. 09 636. 48 16169 84. 14 336. 78 145. 47 178. 83 293. 41 11967 83. 98 1036. 36 258. 41 1617. 83 495. 77 7278 83. 62 1079. 66 205. 71 1408. 78 288. 29 21766 83. 55 202. 85 35. 26 284. 66 63. 71 19112 83. 49 227. 09 41. 26 162. 45 41. 41 247 83. 22 78. 49 23.83 127.29 32.51 18996 83. 22 175. 14 36. 61 124. 78 29. 81 1542 83. 19 741. 70 151.84 1084.13 306. 88 17832 83. 19 522. 94 599. 21 1979. 69 796. 76 17332 83. 07 223. 62 28. 27 303. 15 73. 10 1246 82. 94 37. 24 17. 41 82. 08 35. 89 16168 82. 94 544. 90 152. 30 363. 58 234. 93 3615 82. 64 103. 67 34. 57 197. 88 61. 86 21339 82. 63 81. 54 44. 75 34. 07 19. 67 1689 82. 61 1224. 06 1215. 72 4062. 22 1648. 08 24051 82. 30 75. 09 17. 26 113. 95 26. 52 24821 82. 27 34. 36 7.77 54.32 19.77 3610 82. 03 734. 56 24.13 1122.80 330. 52 1553 81. 63 1952. 70 632. 62 3812. 62 1693. 78 23505 81. 63 790. 51 196. 75 566. 19 124. 65 21648 81. 57 298. 40 58.99 208.18 69.29 21542 81. 48 75. 73 11. 78 53. 64 19. 14 495 81. 45 270. 73 74. 76 127. 48 87. 19 18468 81. 39 106. 55 21. 07 77. 98 27. 23 15393 81. 33 222. 37 28. 91 286. 78 51. 31 18681 81. 30 388. 94 53. 06 282. 82 72. 56 4012 81. 23 1137. 93 352. 70 702. 11 303. 50 25550 81. 11 130. 44 21. 18 99. 94 23. 47 15599 81. 08 768. 89 96.61 962.67 147. 01 245 81. 08 30. 84 10. 46 51. 23 15. 00 3713 80. 93 785. 80 153. 20 1070. 46 218. 25 7681 80. 90 141. 52 29.83 104.60 44. 18 19358 80. 77 230. 36 276. 27 811. 89 308. 44 20876 80. 75 1429. 42 179. 01 2010. 11 495. 92 14638 80. 72 103. 18 17. 90 77. 40 20. 36 24843 80. 63 1529. 74 555.96 2719.25 1061. 12 4291 80. 53 163. 79 60. 20 282. 61 88. 79 9391 80. 47 668. 60 95.16 863.78 204. 49 Table 5J GLGC Identifier LDA Score Tox Group Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 17234 80. 44 450. 62 66. 65 591. 69 138. 75 20741 80. 44 223. 50 26. 65 175. 19 43. 80 23884 80. 38 55. 79 14. 99 30. 14 28. 25 3941 80. 35 312. 71 52. 90 243. 38 62. 94 6691 80. 35 119. 49 85. 12 119. 56 46. 57 19188 80. 32 899. 58 236. 54 1310. 91 334. 70 2242 80. 13 1529. 47 425. 16 2188. 74 547. 68 20714 80. 11 251. 69 65. 33 169. 88 95. 99 2702 80. 11 352. 18 62. 63 280. 79 90. 45 2812 79. 92 250. 95 52. 91 182. 78 42. 75 20713 79. 77 321. 28 83. 43 211. 11 121. 91 18502 79. 77 372. 75 197. 72 765. 58 271. 46 11324 79. 74 567. 08 75. 40 686. 26 133. 81 12846 79. 68 27. 13 8. 38 43. 38 16. 45 15642 79. 43 574. 29 92. 23 434. 05 119. 62 1844 79. 43 215. 94 40. 20 163. 57 52. 46 9439 79. 37 715. 53 238. 18 1099. 47 279. 57 1312 79. 31 877. 80 98. 92 1048. 20 167. 10 21462 79. 31 332. 31 60. 15 254. 18 55. 30 17887 79. 25 984. 05 226. 20 1384. 89 288. 41 20918 79. 25 568. 16 114. 17 403. 50 84. 82 15237 79. 22 243. 57 60. 93 168. 46 37. 30 11610 79. 19 368. 78 38. 57 303. 07 70. 24 6059 79. 07 132. 38 25. 33 187. 49 43. 92 9035 79. 04 153. 86 24. 05 125. 62 27. 03 2782 79. 00 413. 70 142. 88 205. 21 0. 64 25366 78. 91 89. 96 46. 99 44. 98 55. 94 20866 78. 89 654. 18 82. 36 778. 30 119. 91 13004 78. 85 174. 31 28. 36 131. 55 40. 25 21140 78. 79 125. 03 91. 50 108. 35 40. 63 11136 78. 76 832. 19 153.81 1147.90 344. 29 1247 78. 73 839. 48 329. 16 1582. 78 517. 89 25705 78. 67 608. 91 95. 39 477. 51 114. 34 8445 78. 64 50. 64 6. 93 39. 43 18. 79 16521 78. 64 378. 70 73. 70 284. 05 6. 53 3608 78. 46 198. 11 80. 98 358. 92 138. 13 17693 78. 46 1038. 76 282. 54 1505. 15 387. 40 45 78. 37 97. 82 39. 87 173. 04 76. 68 4532 78. 31 171. 23 78. 76 279. 78 96. 10 21914 78. 27 520. 42 91. 18 411. 11 83. 67 1962 78. 25 44. 77 12. 65 26. 15 23. 39 19110 77. 85 342. 86 94. 88 201. 97 95. 13 21575 77. 78 452. 86 97. 04 333. 22 68. 32 19222 77. 73 563. 31 40. 36 635. 63 111. 62 1515 77. 63 246. 92 46. 18 186. 59 43. 06 9073 77. 63 44. 73 15. 30 22. 89 18. 48 573 77. 61 1599. 70 404. 19 2608. 86 1776. 16 16091 77. 52 20. 73 9. 39 32. 57 13. 59 1401 77. 33 69. 28 14. 03 52. 22 17. 29 21147 77. 30 282. 41 67. 81 361. 22 81. 20 15364 77. 24 77. 86 12. 53 102. 74 36. 36 17154 77. 24 245. 45 57. 67 186. 78 60. 02 3454 77. 15 100. 75 18. 92 75. 51 30. 81 15299 77. 05 115. 51 45. 17 75. 17 56. 24 Table 5J GLGC Identifier LDA Score Tox Group Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 24770 76. 96 124. 63 58. 14 244. 33 107. 12 4011 76. 93 792. 94 249. 01 476. 14 218. 70 108 76. 86 612. 75 314. 84 275. 19 150. 60 16881 76.78 442. 88 61. 71 533. 80 110. 83 18887 76. 75 165. 20 20. 55 143. 02 37. 45 3886 76. 75 74. 47 22. 33 42. 38 20. 96 11137 76. 72 1138. 55 218. 66 1635. 07 463. 88 18354 76. 71 704. 94 297. 65 400. 28 242. 40 15576 76. 69 520. 40 95. 90 421. 09 93. 97 28 76. 62 309. 69 141. 93 532. 57 180. 04 25290 76. 53 233. 26 73. 75 140. 64 55. 93 21302 76. 45 175. 69 45.11 245.52 73. 79 17274 76. 44 77. 42 33.89 146.25 65. 82 20801 76. 44 195. 17 43. 72 150. 37 48. 96 Table 5K GLGC Identifier LDA Score Tox Group Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 20848 98.67 1124. 03 59. 72 548. 54 158. 49 15146 98. 61 552. 75 212. 61 125. 29 66. 30 23123 98. 54 948. 44 137. 32 316. 83 113. 69 25747 98. 48 177. 09 33. 14 42. 07 35. 81 14929 98. 39 2578. 08 443. 16 753. 00 395. 31 15004 98. 36 1003. 54 557. 03 153. 76 135. 69 457 98. 36 766. 78 198. 11 285. 03 90. 56 19040 98. 36 746. 18 87. 47 181. 80 113. 32 12606 98. 36 139. 84 17. 95 295. 27 98. 40 15003 98. 33 555. 22 226. 49 31. 19 86. 19 21165 98. 33 169. 51 57. 41 28. 30 24. 49 22592 98. 33 743. 64 93.52 227.11 172. 72 15002 98. 24 640. 78 258. 49 133. 14 98. 70 6416 98. 21 579. 40 132. 32 123. 67 88.39 20582 98. 21 294. 34 14. 97 487. 80 95. 06 17159 98. 15 1500. 61 126. 72 787. 85 215. 88 1501 98. 15 248. 82 53.21 51.72 53.85 22536 98. 15 3172. 12 437. 63 1609. 00 403. 10 24496 98. 09 30. 75 7. 27 111. 42 36. 91 7196 98. 06 534. 14 57. 92 176. 74 89. 27 7197 98. 06 552. 05 97. 28 187. 97 84. 72 22626 98. 06 466. 77 115.62 84. 66 75. 68 1809 98. 03 551. 79 225. 15 32. 34 127. 23 17325 98. 03 521. 47 220. 14 55. 89 101. 96 17477 98. 03 241. 66 34. 05 111. 41 35. 04 6842 98. 00 214. 44 33. 38 110. 48 29. 69 18529 98. 00 501. 19 67. 11 190. 38 73. 93 21166 97. 94 715. 26 183. 98 263. 82 92. 19 574 97. 85 1110. 83 280. 01 349. 51 177. 04 24564 97. 79 141. 81 78. 70 614. 84 191. 71 3121 97. 79 435. 91 101. 84 1290. 92 319. 95 24563 97. 73 53. 16 51.89 321.95 111. 13 14600 97. 67 377. 21 86. 43 184. 44 47. 39 18657 97. 67 817. 51 100. 75 432. 51 105. 51 3493 97. 63 123. 77 18. 10 61. 40 17. 94 8829 97. 57 506. 29 44. 16 283. 09 85. 65 22631 97. 57 1970. 17 341. 41 1035. 66 227. 87 10532 97. 54 194. 55 35. 06 100. 22 29. 27 21796 97. 54 1253. 95 159. 97 690. 15 198. 29 3125 97. 51 134. 07 16. 15 301. 07 82. 87 7804 97. 51 960. 98 105. 31 1652. 52 334. 35 4944 97. 51 322. 82 51. 74 119. 57 56. 74 1463 97. 48 1492. 64 275. 86 664. 70 314. 91 16394 97. 42 1770. 55 477. 74 595. 39 336. 14 16518 97. 39 1674. 58 199. 69 953. 13 316. 63 21391 97. 39 491. 14 76. 01 218. 82 131. 14 12551 97. 39 81. 94 8. 91 164. 20 42. 11 11157 97. 36 381. 78 35. 68 622. 92 138. 68 7307 97. 33 78. 43 11. 40 28. 42 17. 35 23651 97. 33 2999. 14 682. 81 737. 32 670. 73 18275 97. 21 161. 22 17. 79 261. 59 56. 25 2563 97. 12 270. 81 32. 33 158. 90 37. 75 21797 97. 12 684. 25 148. 72 331. 98 107. 52 25198 97. 09 72. 42 16. 64 27. 14 14. 63 Table 5K GLGC Identifier LDA Score Tox Group Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 15879 97. 09 195. 88 18. 98 348. 95 67. 27 20885 97. 06 196. 55 50. 26 589. 85 226. 42 24321 97. 03 278. 42 73. 76 654. 31 157. 88 15032 97. 03 98. 00 17. 89 265. 50 73. 53 17221 97. 03 228. 07 58. 62 528. 15 137. 97 2534 97. 03 70. 98 11. 01 35. 47 11. 17 15964 97. 03 389. 05 102. 49 1091. 29 283. 24 16172 97. 00 196. 13 57. 63 438. 64 92. 11 10241 97. 00 135. 36 24. 60 59. 08 23. 90 14677 96. 97 173. 50 38. 06 69. 76 30. 14 18528 96. 97 806. 92 124. 34 361. 09 159. 22 24388 96. 91 366. 07 61. 09 177. 80 66. 28 20884 96. 88 157. 01 69. 56 737. 17 291. 54 22213 96. 85 343. 29 29. 34 220. 99 47. 39 20457 96. 85 203. 76 31. 70 396. 48 99. 84 10015 96. 85 467. 24 95. 91 230. 34 82. 57 14970 96. 85 103. 48 14. 71 199. 88 40. 65 2569 96. 85 169. 84 58. 46 421. 57 98. 69 20828 96. 82 843. 23 197. 75 322. 31 161. 39 15928 96. 73 360. 97 86. 20 159. 46 54. 19 1460 96. 69 382. 75 102. 15 191. 62 82. 76 19991 96. 66 169. 60 23. 54 342. 07 85. 80 14142 96. 57 126. 88 24. 18 75. 34 18. 27 15089 96. 54 343. 46 36. 17 177. 01 69. 57 17473 96. 51 693. 48 64. 78 442. 45 103. 23 20983 96. 51 56. 90 15. 12 137. 12 56. 79 7414 96. 48 301. 62 37. 09 183. 56 50. 38 645 96. 42 46. 88 15. 03 135. 75 49. 83 13610 96. 30 183. 04 38. 90 365. 50 106. 63 17933 96. 27 250. 36 25. 67 394. 80 75. 13 17363 96. 21 639. 82 80. 77 1037. 93 191. 02 5205 96. 18 86. 34 21. 51 204. 18 49. 25 13332 96. 12 184. 35 54. 35 438. 90 102. 70 1688596. 12 481. 97 76. 93 847. 27 179. 62 4235 96. 03 655. 06 64. 01 411. 65 95. 74 20088 96. 00 216. 81 25. 74 391. 74 86. 08 13723 95. 97 1591. 34 343. 04 844. 53 377. 73 2107 95. 94 286. 61 18. 41 438. 00 95. 36 9212 95. 94 1468. 88 150. 78 909. 30 234. 39 23076 95. 88 225. 13 23. 27 126. 52 43. 88 25064 95. 88 1945. 50 256. 26 1121. 25 327. 07 3995 95. 85 316. 65 57. 49 606. 04 143. 87 7892 95. 72 197. 94 41. 59 93. 14 62. 88 14120 95. 69 344. 76 63. 42 681. 34 196. 77 20458 95. 48 190. 71 40. 37 368. 84 96. 93 968 95. 42 28. 67 11. 78 81. 24 22. 91 15833 95. 39 347. 90 22. 55 491. 39 86. 11 1453 95. 30 123. 25 24. 55 52. 01 26. 39 24643 95. 30 22. 65 15. 29 92. 91 36. 14 1454 95. 27 243. 07 44. 54 107. 34 52. 73 23033 95. 24 416. 40 24. 35 579. 36 117. 73 18074 94. 97 109. 26 17. 39 48. 61 23. 99 9905 94. 97 409. 12 110. 92 745. 80 152.14 25802 94. 94 793. 44 106. 90 521. 62 118. 73 Table 5K GLGC Identifier LDA Score Tox Group Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 1214 94. 88 67. 47 15. 18 153. 85 51. 68 2465 94. 75 74. 41 17. 98 131. 77 26. 88 2368 94. 72 338. 76 47. 77 623 40 131. 64 19824 94. 72 96. 00 24. 52 215. 81 73. 19 646 94. 72 210. 57 63. 36 527. 32 192. 98 14989 94. 54 784. 37 97. 84 533. 89 115. 84 405 94. 48 122. 46 18. 09 208. 02 63. 59 25546 94. 39 236. 19 103. 10 500. 97 150. 34 22910 94. 33 205. 38 23. 87 311. 27 55. 99 15297 94. 24 235. 35 26. 33 147. 28 40. 80 17494 94. 24 137. 15 20. 45 216. 68 41. 79 2010 94. 21 280. 66 119. 92 31. 78 286. 73 19712 94. 12 38. 70 9. 79 84. 74 26. 43 1564 94. 03 1045. 96 352. 70 42. 41 190. 11 17735 94. 00 260. 66 25. 70 179. 21 105. 51 3853 94. 00 89. 36 14. 28 154. 56 34. 31 20481 93. 94 123. 57 15. 86 201. 41 41. 25 1510 93. 94 410. 93 156. 67 839. 46 222. 78 21072 93. 88 97. 50 27. 28 199. 81 51. 39 17800 93. 81 115. 79 18. 77 196. 78 42. 92 14465 93. 69 22. 00 7. 12 55. 40 19. 66 17249 93. 63 662. 67 98. 62 1014. 19 206. 07 4449 93. 57 129. 63 26. 81 243. 37 70. 00 1993 93. 48 86. 65 13. 28 24. 00 17. 68 15540 93. 45 116. 06 52. 11 33. 92 19. 17 12848 93. 39 278. 64 36. 68 431. 16 92. 63 23063 93. 30 242. 82 57. 21 390. 31 77. 53 20816 93. 24 1045. 14 268. 49 407. 56 184. 26 1970 93. 12 395. 31 97. 34 159. 82 57. 55 2629 92. 97 126. 65 56. 54 22. 18 24. 99 4234 92. 87 227. 21 26. 55 368. 61 110. 36 23783 92. 87 303. 32 50. 24 456. 35 79. 84 20849 92. 82 517. 85 86. 60 281. 86 89. 61 3438 92. 81 157. 80 81. 72 149. 25 39. 94 2576 92. 78 43. 64 15. 68 84. 39 23. 87 1472 92. 75 84. 81 22. 82 179. 09 72. 56 1824 92. 72 58. 52 11. 62 110. 12 31. 28 21653 92. 66 435. 18 92. 53 237. 04 66. 87 24649 92. 66 80. 76 6. 94 112. 06 23. 19 17736 92. 57 156. 31 28. 57 69. 99 158. 10 20126 92. 54 206. 98 53. 24 75. 61 46. 32 15850 92. 48 1864. 12 172. 78 1413. 57 279. 10 Table 5L GLGC Identifier LDA Score Tox Group Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 7540 97. 93 486. 02 138. 76 157. 21 80. 71 7299 97. 84 646. 85 211. 22 178. 29 134. 95 4661 95. 47 517. 39 93.47 306.62 84. 32 13614 94. 20 559. 10 110.65 323.06 68.04 14595 92. 40 158. 58 45. 64 77. 34 33. 09 22479 92. 04 716. 72 125. 18 416. 64 126. 59 23151 91. 91 200. 64 48. 10 356. 08 100. 63 15964 91. 55 539. 50 171. 88 1092. 30 283. 63 15411 91. 34 532. 28 101.56 303.52 93.15 13615 90. 34 398. 90 85. 87 240. 22 52. 84 12921 90. 13 225. 68 80. 44 101. 95 47. 41 12979 89. 28 754. 80 237. 57 364. 95 194. 44 21354 88.97 645.15 137.68 417.97 12.5 69 16982 88.41 872.27 500.25 127.82 293. 88 20713 88. 19 613. 63 263.40 208.35 112.71 22619 88.03 501. 19 81. 50 363. 98 67. 50 24321 87. 93 413. 07 112.27 654.29 158. 97 14763 87. 65 304. 65 189. 03 37. 13 142. 64 16521 87. 65 508. 30 116. 48 282. 94 73. 28 24200 87. 65 819. 79 161. 12 425. 21 136. 58 18300 87. 44 220. 58 102. 85 486. 89 169. 94 22698 87. 20 115. 27 56. 59 268. 84 120. 86 13310 87. 15 232. 04 61. 40 124. 22 68. 91 23166 87. 07 254. 30 83. 26 126. 36 61. 00 1894 87. 01 371. 06 120. 65 196. 88 70. 39 22103 86. 70 364. 57 103. 66 219. 40 53. 63 21654 86. 49 610. 80 129. 78 376. 37 127. 86 5183 86. 42 320. 31 60. 86 221. 48 61. 55 6102 86. 24 198. 65 25. 41 143. 71 30. 86 8759 86. 16 246. 43 53. 78 156. 18 40. 90 15191 85. 85 2673. 45 2339. 47 2414. 85 1220. 31 20714 85. 62 475. 80 301.89 167.76 86. 41 15538 85. 56 293. 17 36.37 218.71 56. 03 4119 85. 47 162. 78 28. 48 109. 13 32. 45 3020 85. 38 424. 83 78. 70 293. 70 77. 59 22737 85 25 409. 70 157. 83 207. 21 89. 14 119031 85. 24 118. 24 42. 75 59. 90 50. 43 8065 85. 15 225. 82 45.65 163.47 35. 91 11057 85. 12 96. 32 38. 40 34. 75 28. 49 9583 85. 07 208. 74 101. 61 55. 02 59. 66 20711 84. 95 140. 70 71. 44 33. 55 34. 91 21975 84. 94 342. 10 74. 80 211. 95 62. 48 15535 84. 79 635. 56 107. 51 476. 52 79. 47 20715 84. 77 296. 44 124. 89 126. 05 58. 80 21683 84. 77 83. 44 41. 31 26. 99 20. 17 18678 84. 72 196. 91 72. 64 100. 06 53. 79 2457 84. 67 464. 90 167. 87 288. 94 67. 89 18269 84. 55 548. 35 110. 14 772. 70 179. 32 21339 84. 46 79. 78 30. 57 34. 21 20. 21 16775 84. 32 572. 11 282. 27 1168. 56 397. 36 8202 84. 27 377. 45 72. 53 277. 16 54. 79 17477 84. 19 180. 63 52. 28 111. 57 35. 73 24197 84. 17 107. 40 60. 94 236. 21 79. 34 15679 84. 16 286. 66 65. 08 173. 83 46. 74 Table 5L GLGC Identifier LDA Score Tox Group Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 17516 84. 12 769. 10 139.21 544.65 126. 18 1807 84. 08 1593. 11 543. 91 4019. 95 2715. 05 1597 84. 01 141. 64 66. 96 42. 68 38. 09 6758 83. 67 60. 74 21. 52 28. 80 13. 40 11324 83. 67 525. 31 77. 71 686. 40 133. 36 15667 83. 51 1304. 24 352. 22 2487. 79 1225. 01 23978 83. 49 74. 40 21. 67 112. 19 29. 95 15446 83. 46 502. 42 69. 06 388. 27 92. 25 23712 83. 36 224. 13 38. 61 157. 15 38. 03 16476 83. 27 533. 78 102. 18 788. 60 304. 36 21014 83. 22 324. 17 132. 01 148. 40 78. 26 5295 83. 12 408. 06 135. 30 217. 58 80. 67 6046 83. 07 101. 90 48. 10 194. 33 61. 90 7451 82. 91 502. 98 103. 58 367. 08 83. 19 7471 82. 90 308. 76 49.66 224.13 54.98 14425 82. 88 332. 80 79. 03 203. 82 68. 76 6833 82. 80 96. 02 13. 68 73. 52 18. 72 12673 82. 79 90. 29 25. 44 40. 47 22. 14 21125 82. 76 96. 85 28. 42 152. 75 47. 47 17950 82. 75 89. 75 11. 67 61. 68 19. 97 8820 82. 74 530. 25 320. 31 138. 57 119. 39 1857 82. 73 341. 51 97. 88 203. 31 63. 37 9026 82. 73 109. 55 35. 12 60. 22 26. 27 19509 82. 73 48. 13 11. 49 80. 75 26. 24 14677 82. 70 123. 20 43. 11 69. 90 30. 74 1858 82. 64 264. 03 71. 62 153. 29 49. 94 21956 82. 63 206. 97 23. 50 163. 56 37. 58 14131 82. 63 69. 28 24. 69 33. 77 24. 51 6431 82. 62 132. 49 55. 91 49. 83 28. 54 17088 82. 59 92. 61 16. 98 58. 41 31. 43 15666 82. 57 1060. 02 522. 22 2855. 82 1671. 25 19011 82. 51 487. 88 60. 90 393. 64 86. 49 20522 82. 48 341. 19 119. 99 166. 57 84. 98 21147 82. 43 260. 55 45. 69 361. 25 81. 16 22321 82. 42 175. 73 62. 89 94. 40 68. 17 17357 82. 25 167. 86 96. 71 269. 67 96. 37 24438 82. 21 98. 87 20.24 143.39 40. 54 16552 82. 19 106. 93 35. 18 162. 92 41. 40 23679 81. 96 67. 13 19. 94 38. 29 19. 93 1804 81. 93 1429. 11 390. 65 3161. 94 1771. 85 16446 81. 63 26. 33 5. 45 37. 15 10. 18 24566 81. 55 61. 11 42. 07 180. 55 89. 38 15032 81. 50 153. 02 48. 41 265. 54 73. 91 16681 81. 28 120. 46 46. 82 63. 39 25. 75 23869 81. 20 68. 78 38. 38 35. 67 78. 90 21443 81. 12 204. 24 81. 36 91. 06 49. 71 1422 81. 09 170. 29 61. 30 300. 89 105. 05 16520 80. 98 273. 60 150. 69 86. 32 98. 04 8212 80. 98 2755. 24 1630. 16 2776. 64 1026. 95 16610 80. 56 243. 87 59. 82 165. 05 65. 89 13091 80. 48 52. 53 22. 18 93. 54 32. 42 13004 80. 46 212. 11 74.18 131.27 39. 09 20404 80. 43 94. 71 35.90 45.29 43.92 20801 80. 39 235. 97 71. 05 150. 06 48. 11 Table 5L GLGC Identifier LDA Score Tox Grou Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 15409 80. 33 650. 73 204. 15 413. 05 118. 78 2153 80. 16 416. 39 243. 57 174. 99 148. 74 16312 80. 12 102. 23 41. 22 49. 22 37. 54 28 80. 08 305. 95 229. 49 532. 06 179. 36 9541 80. 05 434. 33 105. 00 293. 71 104. 56 4749 80. 02 382. 14 128. 89 229. 43 180. 48 13092 79. 97 78. 7226. 06126. 1338. 28 4290 79. 94 131. 21 41. 46 84. 46 26. 82 20458 79. 76 244. 63 78. 16 368. 93 97. 12 3254 79. 68 261. 62 54. 46 188. 01 48. 62 1943 79. 66 47. 96 16. 20 25. 73 11. 95 24219 79. 60 487. 67 128. 97 321. 74 100. 36 7197 79. 60 330. 86 107. 57 188. 93 88. 45 1513779. 56 1740. 58785. 791800. 11446. 41 20457 79. 40 282. 98 97. 45 396. 37 100. 16 18713 79. 36 381. 95 48. 08 304. 10 71. 82 343 79. 15 86. 27 53. 27 26. 04 28. 49 4235 79. 08 495. 44 76. 22 412. 41 97. 43 15421 78. 89 574. 98 96. 06 739. 12 153. 32 19665 78. 87 164. 53 59. 70 88. 19 51. 24 20925 78. 68 466. 02 114. 97 342. 39 120. 38 12276 78. 61 103. 82 42. 09 187. 47 61. 18 24472 78. 43 185. 77 62. 80 235. 91 53. 31 18352 78. 40 338. 81 174. 54 155. 29 86. 17 45 78. 36 76. 12 49. 26 173. 08 76. 39 25453 78. 35 158. 39 37. 24 209. 35 50. 63 7489 78. 33 30. 74 20. 35 73. 04 31. 19 1977 78. 29 187. 70 37. 39 133. 15 38. 47 20523 78. 29 867. 83 225. 50 579. 11 163. 88 17394 78. 25 484. 34 116.34 347.89 115. 27 23868 78. 20 339. 24 209. 69 170. 18 283. 60 20961 78. 19 20 76 3. 97 29. 87 11. 94 Table 5M GLGC Identifier LDA Score Tox Group Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 9583 83. 08244685 136.5487393 110.2849532 37. 66760888 13. 19753272 16982 82. 32427648 483.6882478 552.3046692 49. 88186324 32. 90131915 15032 82. 28102403 177.3289571 70.86858812 283. 5409217 59. 40838768 15964 81. 60585161 743.874312 299.3609708 1181. 361174 213. 1612425 12979 80. 3700673 643. 9611477 322.5396617 306. 527439 85. 13902429 21654 80. 32714885 549.4204342 209.6721242 339. 6935388 55. 84290884 19184 80. 29859221 184.5060699 138.4017224 57. 12969511 21. 21914631 5461 80. 12975735 363.2475499 214.8634774 167. 0601785 45. 37528089 23651 79. 97244535 1637.54072 1189.420285 542. 9096823 191. 3034224 14425 79. 31714567 289.2956631 105.737495 184. 9582598 40. 7473309 16312 78. 76788965 101.8624891 64. 40370386 38. 35845782 14. 61990063 22681 78. 67353585 469.7183212 361. 5563587 167. 2478183 55. 584236 23166 78. 55613634 206.8477645 101.4273335 108. 1093764 29. 94389506 1529 78. 52440674 215.9442383 69.39046225 311. 3015724 57. 33641031 28 78. 45860958 337. 7569525 190. 3579737 572. 6706363 145. 8390237 2242 78. 44441476 1562.266609 687.2650843 2311. 300749 401. 81139 7489 78.41251816 39.969397 22. 84173 80. 91009417 28. 09717441 2555 78. 31866535 138.9497043 71.0446582 72. 74579762 17. 34013384 22569 78. 31833136 433.3052164 165.3260103 660. 2852423 135. 0527541 11618 78. 26405705 253.3853136 122.3102383 409. 7968553 86. 37081821 3874 77. 9921845 655.5341186 183.3817932 905. 2090016 155. 1052713 17682 77.92371537 543.6295408 230.3423337 801. 6274752 133. 4359357 4291 77. 81767172 182. 8583968 89.67887639 304. 1338558 72. 33137744 22321 77. 79228804 179.8586879 123.2440901 75. 47084945 26. 5781107 21683 77. 71496802 55.09213984 33.27371704 21. 13344315 9. 738536318 812 i7. 52008149 110.300102 37.74055592 159. 2009582 31. 00283772 15928 77. 50321471 230.6186191 81. 85977686 144. 792893 33. 217028 17361 77. 49 81. 56 9. 55 151. 85 49. 33 3610 77. 34289675 786.5228846 383.1597512 1195. 762426 266. 7672417 19040 77. 34022478 341.4502271 225.2340943 150. 6823975 34. 34075604 15382 77. 33170789 389.1289702 422.3483993 77. 24627235 48. 54365298 6046 77. 32 132. 00 60. 76 209. 20 53. 92 16314 77.26 103.96 76.71 33.61 21. 85 16168 77.11995458 630.283295 458.341233 308. 4957265 64. 72400923 12978 77. 09123094 161.0616731 78. 8602948 82. 73480249 24. 06911838 8721 76. 93057898 122.2361625 61.9077009 198. 8519365 58. 96316989 21239 76. 71932666 181.7185987 94.60956961 89. 35257633 26. 32116899 3091 76. 72 545. 67 168. 85 749. 73 128. 16 13610 76. 70479785 274.9562845 90. 96833619 381. 8322514 61. 62951755 14970 76. 68191914 162. 2102141 48. 9266423 210. 6102648 31. 30381828 22929 76. 65586747 487.9160657 270.6330491 875. 0391787 272. 829724 15299 76. 64785157 136.3012386 106.157285 61. 66374238 17. 88937389 3050 76. 59 151. 97 82. 62 77. 07 24. 98 17325 76. 58205441 189.7373516 208.0626111 31. 0587134 24. 22087464 24219 76. 53329103 444.4375114 155.5594702 293. 4620384 58. 4499819 14929 76. 3703011 1275.172779 801. 0896181 653. 6952264 132. 6222434 6641 76. 28696916 306. 0713042 88.62194155 420. 6952038 68. 81743517 19723 76. 2759473 128.2970893 90.41070177 60. 09331086 19. 39755748 13151 76. 2443847 1189. 02038 539.5803104 699. 6056428 197. 7526277 15300 76. 21582806 266.4468852 233.7031532 96. 87648497 38. 58692577 16756 76. 03547035 221.6236525 72.76140952 160. 6260948 27. 82533344 17161 76. 03263139 1821.710174 615.9155321 1215. 712544 234. 8577001 9053 75. 99806282 188.4077043 54. 90371237 248. 8278068 39. 5416499 20458 75. 72902924 275.504871 100. 5231472 389. 1120081 82. 94622112 Table 5M GLGC Identifier LDA Score Tox Group Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 6638 75. 69462768 69.35965051 25.19842597 99. 4446383 21. 49763394 24431 75. 66373307 140.4973047 186. 7414923 42. 63904535 13. 19878574 15110 75. 64870326 524. 7385351 161.2970513 744. 3958487 164. 5366762 24200 75. 62916451 597.8931172 203. 1549298 387. 8593222 82. 09773986 3875 75. 61 354. 67 119. 89 510. 04 111. 81 7936 75. 6144687 108.4356886 31.04246293 144. 7023827 27. 85248861 3823 75. 50 654. 04 216. 61 458. 26 76. 00 20848 75. 49473122 739.8558427 245. 0915553 506. 9787921 87. 26939539 1246 75. 4800354 51.06050058 35.73888552 88. 19304576 29. 97104786 3995 75. 44012291 463.5694638 147.804498 633. 8236834 110. 344027 1460 75. 37749871 290.3524955 157.0068948 170. 5734639 30. 83287626 574 75. 37182078 578.2333054 363.7499773 306. 4754643 52. 52429358 18300 75.28548287 313. 2217374 163. 4937659 527. 1882256 147. 3671747 2905 75. 27729998 347.6900677 151. 3778017 208. 053687 61. 26056458 22197 75. 25726023 157.3709099 70.51415356 101. 3246948 27. 03541912 21147 75. 23404753 286. 2720645 82.6150118 378. 7980181 67. 04188806 15330 75. 22252467 58.49125065 22. 6188477 86. 8547667 21. 0269227 21391 75. 21166981 385.8061478 231.5126036 186. 3801082 64. 9269088 9905 75. 17125633 584.5801895 181.1793745 780. 6799824 116. 1344345 20056 75. 15121658 244.8044459 87.51577736 328. 9803149 56. 49987294 22612 75.13100984 343.7327296 116.5116157 484. 2960858 98. 80695732 23868 75. 06003574 476.5917806 578.566726 104. 3862329 73. 16177261 14458 75. 02262821 66.07115821 38. 46172099 29. 15168483 17. 52209128 24237 74. 96551494 89. 34383693 56. 62184758 42. 92380577 17. 40618436 14424 74. 93411934 239.4400853 296.6620083 40. 59217046 37. 53029959 17401 74. 88535596 1485.695027 694.8549568 908. 508536 210. 902772 18906 74. 86197625 170.7813444 84.29130131 280. 2632832 81. 29656617 13611 74. 83642558 171. 0261776 92.33219744 268. 1311179 69. 5925432 5601 74. 82 640. 28 294. 69 934. 56 178. 65 7299 74. 79100215 340. 4805627 256.9208944 144. 5353128 52. 30383717 12921 74. 78231826 160.5493302 75.66485918 89. 60925607 28. 73773092 4463 74. 76762245 101.5953476 62.27587437 161. 6717233 53. 31108112 8143 74. 69080343 104.7695109 84. 13921659 29. 09088827 30. 02739607 10818 74. 69046943 290.080445 197.297128 507. 055784 156. 484313 23538 74. 65656886 187.0143437 128.8639475 88. 48179831 33. 56740662 4944 74. 64504601 188. 8391331 90. 79119087 105. 8633001 33. 59442944 15111 74. 61314941 829. 5271044 273. 3268883 1166. 379712 236. 6780581 10985 74. 58459278 800.410809 240. 2270404 1100. 953535 203. 6618654 17357 74. 57323692 177.8296623 108.4523586 287. 6047245 80. 31450427 17908 74. 56789299 121.3571079 116. 1216261 42. 52999623 16. 5484268 4330 74. 56171407 347.3358307 137. 4559711 482. 9800669 108. 2803404 3121 74. 54468028 959.6912721 406.1173378 1369. 205783 250. 5821685 23299 74. 52480753 468.8078098 165.8361914 330. 3112996 69. 58410495 20161 74. 51345168 72.01468121 53. 68059035 25. 31805526 16. 61070956 15089 74. 51328468 251. 3256155 99. 68382039 160. 3812585 49. 67999362 20457 74. 51311768 307.2459887 108. 9163745 417. 6507608 84. 51558942 22592 74. 45049348 441. 3278412 302.5254789 185. 7428044 92. 86088318 2102574. 37313. 31 107. 42 441. 97 94. 86 20830 74. 35313372 763.4705375 278.5082765 513. 0660947 135. 9445144 23261 74. 33008801 1167.643034 374.5231911 1601. 584279 272. 589167 15618 74. 28733655 115.8554442 40. 3151267 80. 50306764 17. 75243271 1422 74. 27831867 203.5115649 89.60232364 319. 0362239 84. 83935923 5863 74. 19832668 106.0616484 33. 34272725 146. 2567669 29. 69099415 6804 74. 10681184 789.9900816 408.8443154 1302. 23147 346. 2547845 Table 5M GLGC Identifier LDA Score Tox Group Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 15986 74. 09829495 229.6581874 101.2853036 339. 5941441 70. 48693419 18360 74. 08076017 154.4788107 47.05055977 214. 393766 51. 15202013 12349 74. 04652561 196. 4837332 54.09188201 244. 5657486 51. 7956927 13609 74. 00076819 176.8117791 58.87359803 251. 9175082 56. 78328918 19678 73. 99809622 44.46188591 60.23324179 110. 3513435 45. 83978038 1727 73. 94699487 105.4102508 122.46824 22. 29966809 20. 76306568 18337 73. 9209432 1205.405107 398.898709 1647. 906831 276. 5380239 4479 73. 90691538 235.8144938 118.8454211 131. 9693374 56. 66432098 12961 73. 90073646 137.3492423 37.56911937 177. 0745243 32. 15894315 15879 73. 8893806 284.5730052 70.16546857 362. 8390325 59. 90658185 7540 73. 88403667 252.9068785 154.8627671 138. 9588658 33. 26393784 1462 73. 80103873 698.281705 424.3668671 379. 7373024 81. 29117089 15002 73. 72672467 244. 2298557 206. 548638 112. 5697128 27. 72152824 13727 73. 69182211 67. 87259725 42.11981673 119. 1840195 37. 60278063 15955 73. 57 515. 14 191. 35 728. 18 122. 31 20035 73. 51781032 306.7725912 177.3556465 157. 6016663 53. 16881717 8339 73. 49175865 292.7362043 124.6264371 423. 1068251 88. 76931187 811 73. 48324176 192.9770905 69.9330111 265. 1530947 46. 48636774 7101 73. 48 1028. 63 1448. 92 269. 03 75. 33 15039 73. 40876071 191. 9823051 102.7247359 287. 9523913 78. 10921214 3822 73. 37469314 1222.471751 463.1311279 866. 8616534 181. 1339295 3959 73. 36600925 453.5922062 139.9476597 330. 9248233 74. 21747797 4952 73.3546534 155.5933788 74.76467916 95. 46100924 25. 88868161 13411 73. 35114644 525.6540474 243.9929933 878. 9727098 298. 4088281 24496 73. 34864147 77.53936584 41. 56582163 118. 8841241 29. 67076515 23978 73. 34279655 86.92932267 32.18783863 116. 828879726. 49810705 11483 73. 32041883 116.3027555 97.07083281 45. 19525799 13. 89151735 22885 73. 32025183 1845.034431 706. 0839859 1184. 427221 338. 8455491 4440 73. 28 210. 00 74. 37 306. 59 75. 86 2195 73. 27115446 58. 1346164 36.41544415 94. 82246526 34. 85537693 20694 73. 25712663 743.8512961 251.4832563 959. 0486315 180. 735879 3467 73. 26 477. 56 179. 67 670. 32 151. 77 14677 73.22 105.84 49.33 62.34 18. 47 6487 73. 18247858 87. 46073345. 24.66936209 113. 1656478 25. 19154745 3608 73. 17680065 234.714193 128.0553145 383. 4977487 124. 1499765 23203 73. 16243884 136.4482476 40.60846178 175. 9440252 38. 17308244 10887 73.15091598 45.59776079 19. 26180792 68. 18660382 20. 96287878 12561 73. 12536531 102.2762346 52.56512622 159. 1250387 45. 41988674 15663 73. 11718241 250. 3325832 89.69920875 172. 228523 33. 35386467 7196 73. 11150448 293. 5589143 170.4462218 155. 3520027 40. 04001176 11164 73. 11 349. 24 142. 19 507. 35 120. 35 394i 73 0941367 308.735741 77.67557449 230. 069061 48. 84198107 22554 73. 07392996 415.0183429 141.5557663 556. 6455466 106. 8579765 13343 73. 06808504 157.2067443 46.99161278 208. 9077432 43. 13164312 12332 73. 04537332 411.1613085 193.5891409 580. 8890108 134. 5335609 7128 73. 02817254 239.1426458 69.19063177 314. 3465504 55. 04435889 794 73. 02800554 149.9988713 59.20316287 220. 6178599 54. 39878992 21632 73. 02550058 81.27734286 68.17005823 21. 99813036 38. 2953058 19031 73. 01998965 115.0485875 95.43994528 48. 9126224 21. 82538707 20828 73. 00846679 502.2473423 271. 1834974 284. 5311051 92. 4929031 22101 73. 0081328 95.0688379 89. 97980952 187. 4798581 72. 68823613 17477 72. 96554834 152.2283562 61.41721729 103. 9500869 20. 61868868 21653 72. 94266963 312.5412982 114.3057351 222. 6382613 40. 97720451 4789 72. 94250263 59.69316361 25.79130654 36. 25017547 16. 9263929 Table 5M GLGC Identifier LDA Score Tox Group Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 24568 72. 92747282 100.9854279 45. 77643689 166. 3747268 65. 68252702 23202 72. 92496785 121.8218073 37.4223132 164. 3583568 35. 739692 25453 72. 91945692 169.5385768 55.06858446 219. 2370093 42. 22252817 13634 72. 91695195 1089.909525 505.6176099 708. 2744112 127. 1635939 9673 72. 89039929 41.62752139 23. 9624369 67. 9158819 25. 83115298 22626 72. 88555635 183.9210533 157.8210185 66. 65379062 23. 30181235 13349 72. 86251065 172. 7498279 55. 72890499 123. 9271713 27. 77975703 8829 72. 82527012 370.3425049 120. 1345988 265. 08681663. 71656822 15051 72. 81 870. 06 414. 32 531. 84 140. 63 17771 72. 79387452 987.2353328 409.5437444 656. 0935041 156. 8142212 14484 72. 73325429 334.2823847 89.84388565 437. 9713071 96. 59005867 14185 72. 70803761 286.6012774 150.7172826 168. 4541254 57. 75119127 18529 72. 64224044 279.8103006 134.5542568 172. 941485 39. 31168364 23946 72. 63038359 163. 7394849 60. 22818988 222. 3458685 52. 09881666 17159 72. 53636379 1017. 46374 356. 3241579 743. 4742457 134. 8926558 21443 72. 53068586 141.5087876 81.92489411 79. 90222801 27. 46553869 5855 72. 51882901 48.54935197 31. 99643857 74. 57794713 25. 25898096 13618 72. 50196223 131.446852 42.43820367 95. 49719596 21. 0584271 12716 72. 48993838 131.6741256 35.67214558 169. 4946023 38. 20699186 17550 72. 45587081 986.160813 374.7937126 1326. 286035 307. 3041885 5474 72. 45002588 535. 2923376 201. 9471092 756. 7417489 194. 0568571 5711 72. 44701992 273.463279 99.04844473 392. 0601198 106. 5505539 2912 72. 39291261 1931.737359 615.063966 2564. 077466522. 3042249 9017 72. 38122276 76.73353212 33.16762831 116. 2884854 36. 84832913 6059 72. 36118301 154. 2019464 39.08353915 195. 0358442 41. 70427967 1501 72. 33913929 109. 7890806 98. 72204686 39. 88217718 21. 66435281 8188 72. 32127052 307.4560841 113.435179 412. 5977746 118. 9863598 23195 72. 30156477 232.9214407 106. 7475078 322. 6563231 70 : 56526638 728572. 30 183.98 45. 26 227. 37 39. 94 21458 72. 29321488 333. 719882 163.5279209 208. 7840327 68. 3434868 23957 72. 26165228 111. 136839 62.08098358 56. 84170567 26. 48020347 7784 72. 19284915 562.8262904 162.4051288 718. 7859352 107. 9257063 6416 72. 17 221. 69 181. 98 105. 92 33. 73 19679 72. 16997044 554.0548312 249.8434896 799. 208115 160. 2227266 3916 72. 16429251 521.2494374 191.635131 693. 1755282 117. 6873361 24388 72. 16 256. 14 119. 20 163. 06 35. 67 4235 72. 16145355 511.7131741 134. 644402 389. 7019942 70. 87532979 17196 72. 15544163 105.3599138 26.38579321 132. 0773497 22. 43465669 21462 72. 1414138 306.539429 72.05119023 242. 5457166 45. 94897687 1510 72. 14124681 644.6907685 250.3002812 882. 9239564 187. 473853 2348 72. 13807385 327. 6327036 189. 49475 501. 69599 190. 9571321 17524 72. 1098512 874. 8824969 306.1319417 1156. 444814 234. 2742269 10464 72. 10116732 93. 88361398 31. 76228943 126. 6499333 27. 52656727 7127 72. 10100032 189.6279016 95.06964563 284.503156 81. 78200409 21882 72. 03520315 626. 539768 164.7108169 793. 6760678 153. 0810134 17339 71. 9294935 1792.985725 669. 1390035 2389. 414771 537. 6641779 10015 71. 92414956 325.4652102 153.5765557 212. 0585252 42. 32926652 20801 71. 85 199. 99 73.50 140.35 32.13 7888 71.84 318.41 78.58 247.97 40. 89 17256 71. 80658306 324.8525266 154.4265957 449. 9846896 98. 32616047 22930 71. 79455921 198.0132602 107.4265272 333. 5952638 130. 8979194 3049 71. 77535445 291.7940055 154. 6257178 166. 9363278 53. 28371204 17734 71. 76 206. 37 202. 42 95. 30 30. 54 20082 71. 732436 92. 49771136 42. 32852743 59. 76248687 14. 71505541 Table 5M GLGC Identifier LDA Score Tox Group Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 4327 71. 732436 124.904039 64.17386639 73. 50786335 19. 33196751 18271 71. 70638433 622.1754394 201.2914108 765. 3878724 134. 2823131 1141 71. 70371236 310.4547546 97.82116884 226. 1620877 48. 17094826 3713 71. 69770044 870.0920545 222.4658473 1118. 081047 183. 6493294 7537 71. 69469448 182.2977249 58.80458232 237. 2841089 52. 87814656 22596 71. 67799469 80.40368647 26. 06975968 58. 43304066 14. 91196991 4360 71. 67214976 269.7964439 91.90423108 345. 4475402 58. 55070595 1081 71. 66630484 413.8169497 133.9204914 554. 0918883 106. 6621528 2702 71. 60084167 366.9630027 146.7576451 258. 704476 48. 99924667 354 71.60 342.25 192. 43 190. 95 42. 15 5199 71. 58898482 426.6781047 194.5965508 588. 2380815 150. 0565394 25747 71. 58380789 77.46426615 61.56836353 34. 93635566 16. 33129208 13633 71. 57228503 490.859187 292.9104741 281. 7702118 78. 21967829 20003 71. 55424926 27.26624376 18.63775544 51. 09157179 22. 27713208 25198 71. 54923932 41. 83738407 21.30414887 24. 46897318 10. 2887544 5481 71. 53187155 91.61281005 65.17050178 28. 14592964 47. 24102799 13332 71. 4802692 348. 318777 115.9413156 459. 9662366 88. 50144973 6321 71. 42616189 574. 0456997 185.5861715 430. 1525559 101. 4344889 4473 71. 42599489 131.0465748 57.9009332 181. 2716922 41. 7246204 405 71. 40862711 163.6570742 53.25338415 214. 369048 52. 02616005 23872 71. 40645614 128.3896922 182. 3235051 24. 91985805 23.80373187 18302 71. 39142633 60.93274749 77.95488674 124. 3849227 68. 01025453 15042 71. 38341043 113.7848867 77. 4706215 57. 27629582 27. 29420376 6382 71. 3775655 168. 3590284 54. 66912751 117. 2240917 30.5916709 1409 71. 37422555 356. 3482649 100.2570505 457. 0897876 90. 41166982 10130 71. 36303669 174. 0633085 65. 67212316 230. 5180359 47. 39273862 21125 71. 34867487 116.793056 56.17889018 159. 8219905 40. 70025457 20481 71. 33147409 164.2250117 44.84688901 208. 9019923 36. 59950412 16859 71.33 166.91 73.19 112.81 33. 48 16147 71. 31427331 133.2713322 41. 16539683 174. 3821982 34. 98987877 9699 71. 31143434 40.800459 21.59336067 56. 86011612 17. 18231905 10789 71.31 226.28 98.93 319.54 77. 45 6796 71. 30592341 237.5148442 61. 53051141 182. 3973545 44. 66569526 410 71. 28855564 870. 9734112 244.8206654 1083. 444257 197. 6148927 18564 71. 21123562 177.1818749 50.68623343 222. 8971499 43. 2196108 12798 71. 20856365 127.9179407 41.67147705 161. 9583087 30. 85329433 15004 71. 20 315. 68 341. 04 126. 60 39. 41 21318 71. 1972078 71.28904452 31.21133472 42. 85410721 22. 48605551 6039 71. 14877841 398.0605484 140.8521054 292. 5555827 43. 87001826 18792 71. 14527146 105. 5641832 35.06965105 140. 7557808 34. 59681697 15642 71. 13725556 552.6908782 175.7519777 408. 6795547 83. 65679612 12812 71. 1339156 71.16451798 36.21027548 103. 4513266 31. 81785501 14996 71. 11671482 339.3300514 143.9979671 507. 2107686 153. 7067385 498 71. 08865917 683.2994891 214.007319 507. 7755444 92. 92888055 10087 71. 08548621 1154. 31678 346.7061181 1463. 958309 251. 6377099 12331 71. 08264725 472.782575 167. 0649748 617. 169582 120.6867211 8477 71. 07145839 659.0457127 204.6617645 463. 617062 103. 0264273 13954 71. 06 948. 19 350. 16 1298. 60 301. 79 17907 71. 03 1012. 87 306. 06 1257. 12 200. 00 22656 71. 02269501 175. 5960199 69.44916713 113. 0049246 41. 69051937 2370 71. 01401112 915.6984826 221.2013897 1099. 411882 156. 5781346 10016 70. 99714434 301. 5274805 145.9792275 190. 3539826 43. 03506275 18269 70. 99380438 637.3872989 170.1980876 810. 1018171 163. 937515 22928 70. 99347038 162.5453963 62.7086771 235. 9206416 78. 67137638 Table 5M GLGC Identifier LDA Score Tox Group Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 24321 70.99 515.86 195. 77 686. 86 131. 04 23512 70. 98812645 828.9897486 249.3344159 1077. 375262 203. 7223722 7903 70. 98528749 350. 5453484 194. 23864 521. 8749865 172. 1493708 6336 70. 98 336. 24 89. 69 418. 43 89. 90 11967 70. 95 1213. 17 570. 43 1709. 91 412. 19 11708 70. 94270303 386.8003922 118.0261743 291. 4028205 61. 61537016 20849 70.93418614 372.7188256 145.9724592 262. 8478403 56. 35553021 20086 70. 92550225 176.2588503 100. 9839636 94. 57079689 56. 93242072 16775 70. 91949032 829.8082119 416.7547122 1259. 056219 355. 5379472 1698 70. 92 172. 23 191. 95 50. 55 32. 52 14095 70. 92 281. 28 79. 38 369. 45 63. 47 676570. 91665136 585.0367365 187.8003804 763. 3969282 148. 4962585 1581 70. 89978457 84.40443826 27. 89534583 62. 31427166 13. 19097482 22820 70.89410664 288.1190696 111.4524723 200. 7418441 47. 57591793 5990 70. 85953808 366. 3519689 68.11041757 308. 364785 51. 8240886 22747 70. 83933134 74.14874761 30. 31242787 98. 18564151 26. 53935912 21885 70. 82196356 142.8105941 40. 75769988 189. 0843655 42. 6957976 3079 70. 79674688 63.04721313 43.40895794 28. 63200188 23. 267219 5923 70. 79674688 483.7836606 173.4808852 620. 2452282 121. 7386925 14867 70. 80 101. 12 6. 31 165. 12 71. 18 19235 70. 79340692 763.4928387 289.1267594 1038. 844606 281. 3859308 7690 70. 79090196 257.5909963 97. 89101874 171. 849413 74. 75028528 13111 70. 79056796 174.860056 60.32230683 227. 4712045 55. 77617287 1159 70. 77654014 806. 917713 265.6053539 1032. 085281 192. 0252292 9781 70. 77069521 92.58980656 36.11235607 127. 638116 32. 75832457 17393 70. 75399542 204. 124932 109.1717801 121.382968 33. 63659555 5329 70. 7476495 33. 30547604 19.24667641 51. 50320834 17. 81606651 3878 70. 74197158 403. 2347516 111.4733788 513. 4119933 109. 3514016 9468 70. 73913261 42.8674446 35.25182606 68. 53373052 31. 39077316 353 70.73 272.05 161. 59 149. 39 40. 00 21305 70.70456405 335. 5403178 107. 0804394 461. 1318069 122. 4271664 4462 70. 66481856 730.6257892 304.6597778 995. 431334 245. 7726301 19768 70. 64511281 963.1099008 248.7687166 752. 6982114 130. 8907506 17807 70. 61939513 1025.458861 284.1245566 795. 8935405 128. 7916384 7279 70.58 177.33 131. 04 191. 37 58. 86 23961 70. 54775304 666.1151134 193.4003866 805. 831464 112. 8350419 16520 70. 54240911 132. 8613946 84.96659613 72. 6601183 44. 25249046 17499 70. 54190812 50.17968339 30.54421913 22. 00448366 22. 12875837 14790 70.5272123 109.4097569 74.61549723 185. 3000757 76. 25523345 691670. 52470734 317. 8219585 111. 0268929 408. 6141486 85. 19381033 11974 70. 51318448 172.0478497 92.75009213 244. 794786 74. 37487748 11455 70. 50 162. 65 95. 78 94. 80 26. 70 7543 70. 49564971 178. 547379 78. 57317657 269. 0421232 91. 30723273 12467 70. 48 91. 52 43. 59 57. 64 16. 70 17684 70.48178888 183.8798358 61.31828646 243. 7559457 49. 96031474 17438 70.47026603 26.7382404 45.54097206 57. 63231313 34. 17013966 13176 70.47009903 46.41799018 20.28410744 65. 32124446 19. 51464161 275 70. 45339924 453.7148571 254.4387856 576. 7986868 132. 1872501 1402070. 44212. 8056. 70266. 0146. 38 3430 70. 43636546 621.1802909 275.8648069 418. 2233015 103. 8022286 6518 70. 43619846 144.0774161 37.08502734 112. 7147406 24. 8752467 18303 70.44 281.64 239.24 513.56 243. 07 5867 70. 42 195. 07 60. 67 148. 14 26. 48 692770. 39010705 264. 7935922 87. 90568922 348. 9047929 78. 75748433 Table 5M GLGC Identifier LDA Score Tox Group Mean Tox Group Non-Tox Group Mean Non-Tox Group SD 25070 70. 38994005 353.201825 90.9057057 442. 8817225 89. 01735385 12587 70. 38426212 172.8425554 49.41038279 225. 0384086 48. 36937066 20865 70. 38142316 235.5178941 58.52316469 291. 3112086 53. 15153075 24236 70. 36472337 98.10809021 31.96761671 73. 04437691 15. 28584669 16684 70. 35620648 709.3649229 236.7375456 508. 8945621 112. 4304221 9452 70. 35069555 245.7617883 292. 6221619 114. 9709603 32. 36274589 4199 70. 33583273 447.7856929 168. 99085 592. 8718764 144. 2735394 11454 70. 33 328. 59 156. 12 216. 73 53. 33 21796 70. 32764984 888.4017259 360.4669486 657. 7468182 113. 1481704 19998 70. 32 192. 15 78. 72 267. 63 67. 09 1399 70. 32 291. 48 158. 06 180. 41 40. 15 146370. 30477113 1010.906056 562.2315641 597. 6285113 147. 5163605 8599 70. 30143117 289.7102636 121.7540684 408. 8106404 103. 3414894 19067 70. 28423039 126.0808384 48.73348414 169. 7256121 43. 06255744 24235 70. 27621449 713. 0504022 392.6566221 431. 1344096 115. 3208855 5295 70. 27320853 300. 3673 122. 6395005 200. 3777563 56. 99205768 17157 70. 27036957 66.74546809 35.9806367 40. 40264137 14. 12606346 24762 70. 26986857 718.3765021 276.1477473 983. 3177792 297. 9605419 22599 70. 25600775 66.34406284 31.76809853 41. 24936186 18. 37197756 20829 70. 25032982 1242.416049 483.5054646 851. 3168509 199. 4060102 1885 70. 2439839 271. 0949115 74. 76518095 352. 5464662 81. 05516141 7700 70. 23329604 122.8595378 82. 18167819 72.07968292 16. 69398572 6711 70. 22995608 67. 6521358 24. 44261842 47. 10757143 22. 07497066 22328 70. 2127553 317.0894814 111.2229989 404. 0684734 93. 91538499 13392 70. 19872748 239.3228528 71.29262811 181. 6550147 37. 08840136 1798 70. 18970959 258.6239005 95.82095389 346. 7327101 96. 88717299 9114 70. 1811927 693.860219 204.9305374 879. 8300873 192. 7878948 4933 70. 17618276 388.4071663 424.0827485 93. 57485666 104. 1871857 25777 70. 16465991 731.1269475 475.1048291 385. 6387638 125. 2433796 5565 70. 16131995 296.7569975 131.2082754 413. 3646434 102. 2345034 17420 70. 14679114 61.25008761 32. 17535043 94. 12664744 32. 93397715 7872 70. 14111321 85. 7718341 33. 42042032 118. 8883017 31. 24593067 19085 70. 13593627 94.39700898 39.41352311 61. 50537192 14. 57063483 25567 70.13309731 673.5066146 317. 8219004 438. 9509529 133. 112788 21024 70. 12675139 455.6164345 93. 77946063 553. 7599162 96. 12838839 21105 70.12124046 249.5365471 66.25713529 312. 1801594 54. 80674377 4661 70. 11873549 388. 812595 126.7826634 288. 3700687 54. 8123755 6635 70. 1182345 193.7443247 78.12105317 263. 6595233 72. 24389761 16708 70. 11255657 207.7538048 51.36507757 256. 4151971 46. 44776023 2250 70. 09836175 1118. 061362 305.4698352 1406. 389129 242. 1009635 9067 70. 09568978 803.7783177 204.3856207 624. 9499096 138. 7609652 15146 70. 08166196 203.6218298 143.5123436 112. 756109 37. 18053855 1478 70. 02972562 270. 2709361 105.7728946 371. 6625226 79. 43883267 406 69. 97528431 313.9225633 96.71895909 398. 3675185 80. 50659235 24234 69. 97010738 302.5101331 219.1370069 168. 0694456 50. 6457125 20493 69. 92969389 391. 4896341 143.6531328 510. 9476405 105. 1896405 4178 69.84652895 527.8687514 134.5334345 640. 2250757 119. 9461864 45 69. 83517309 120. 9649065 88.26258123 186. 4908089 67. 03141815 1454 69. 83 155. 56 72. 94 98. 16 40. 12 25379 69. 81830631 91.36952894 33.44083062 67. 37191422 14. 99700037 11692 69. 79192064 1135.765908 414.4834877 1546. 524472 408. 082855 19086 69. 76970992 146.2982894 67. 62426161 91.90156365 25. 25. 40768257 17447 69. 71510162 757. 1092798 315. 0026535 1014. 03074 248. 7855862 5497 69. 70658473 618.3891525 241. 8729868 823. 9281494 151. 3202488 Table 5M GLGC Identifier LDA Score Tox Group Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 23194 69. 65498238 62.69622659 24.81693426 41. 16752769 22.21797666 19 69. 62943171 426.8830038 118.6334492 336. 4255709 62. 63947723 11849 69. 60087507 948. 1751709 279.8387309 737. 4883024 123. 97332 3465 69. 59753511 210.0319804 70.48668178 271. 4668918 62. 44793967 1993 69. 59519714 43. 10184781 30.86190782 20. 51127087 10. 4903739 22662 69. 52 107. 46 29. 01 136. 36 29. 33 18452 69. 51754313 321.3878641 118.9110657 424. 391574 94. 62603068 17324 69. 50618727 312.5926635 107.1245732 383. 7679626 72. 29693664 744 69. 50602027 282.8384135 77. 81116212 353. 1333504 70. 01135148 19943 69. 50318131 284. 2980177 126.3869505 383. 928817 104. 8721705 13930 69. 50084334 214.9089308 153.331537 106. 240643 42. 57434118 22539 69. 47729664 36.74107571 37.02283507 67. 50720611 37. 70265225 16476 69.46894674 661. 9654825 207.0570396 807. 3400046 148. 2467882 20753 69. 46059685 146. 9881391 38.9952964 114. 6096864 22. 23178425 7197 69. 38344383 282.3300938 150. 9619233 170. 1503853 54. 40399664 556 69. 38260884 55.50132335 17.48087181 75. 27571431 24. 04221562 4198 69. 32015163 622. 3402992 199.7713179 799. 2132627 160. 4720245 324469. 30595681 95. 06917614 31.63411195 119. 81669 24.27866027 23063 69. 28291111 328. 2658823 83.6090783 404. 561604 68. 57292929 24264 69. 24567058 26. 11217385 22. 43333372 43. 28478863 18. 55868879 2153 69. 23765468 324.5935101 302.l8245339 143. 8406632 45. 13859767 5496 69. 23448172 508. 9524014 208.9382494 686. 2856793 135. 7152932 452969. 23130876 67. 85449471 27.85368995 90. 38311629 24. 2100319 2235269. 21240. 63198. 59 129. 5552. 38 22537 69. 21410798 218.5350397 146.7680792 320. 5449701 127. 5696536 1430 69. 19139627 91. 40795716 91.79231802 157. 3163186 82. 8694698 12276 69. 14563885 146. 8290814 72.19394428 197. 3180931 55. 12187566 408 69. 14246589 130. 3805348 67.27728587 191. 4580768 65. 83246181 14184 69. 13444999 138. 8526752 74.21831436 90. 86184089 35. 50680695 5837 69. 05412401 707. 5200515 227. 3360419 877. 5856354 176. 1594803 19152 69. 04293515 209.4889223 82.42495052 150. 4710597 37. 99742228 24648 69. 01371053 23.19157675 11.6951982 35. 71395341 12. 84500013 291 68. 98264892 188. 6257241 56.90927233 232. 0130777 38. 28705897 409 68. 87944423 803. 4588849 193.8990371 969. 1247908 164.618582 20816 68. 79995324 595. 8358273 369.9222458 370. 4656146 83. 63140389 20449 68. 79711428 100.4900488 132.9211559 33. 15487613 21. 87043029 23445 68. 77089561 516.3551752 187. 237735 686. 2066418 139. 3621424 17494 68. 73933301 185.7094369 45.48548725 223. 0254103 37. 74558387 24438 68. 73064912 114.0695333 42.85206114 148. 9829095 36. 09924566 20817 68. 72 1865. 76 1135. 85 1150. 17 447. 11 25705 68.6853927 571.3566592 176.4043974 451. 9728048 76. 32131489 20414 68. 68171874 85. 25065547 29.1778343 114. 5185098 31. 66919651 1712 68. 61658957 209. 6897328 68.60632447 160. 3879218 35.87902845 13646 68. 60523371 999. 5515778 297.3365691 776. 9704191 122. 9631955 18301 68. 5671582 62. 34075661 33.80497723 100. 8072372 42.70710806 18070 68. 56181426 29.36749701 21. 99959698 48. 21170897 19. 38594154 15191 68. 53075266 3290.474496 1751.223512 2180. 500127 805. 9269968 17473 68. 52507473 517.999113 161.8598317 427. 536449 71. 9934835 21053 68. 51839482 66. 73426419 31.71787962 102. 8261937 48. 28425026 22196 68. 4878342 63.01977878 25.81558037 44. 76996899 14. 72142187 14309 68. 45844258 112 8770993 71.13031295 191. 135603 83. 9940291 18741 68. 45560361 22.45924623 9.465804661 31. 4249201612. 24548318 18011 68. 45359964 55 32740853 47.59398519 21. 92483457 18. 1624083 17269 68. 45025968 556.6625611 223.6922613 748. 9429353 194 3156688 Table 5M GLGC Identifier LDA Score Tox Group Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 4589 68. 42738097 1175.409579 346.4630047 1472. 99309 302. 8077957 19469 68. 41903108 301.3400452 113.0311594 382. 8696906 90. 3486576 21145 68. 41853008 166.4457933 59.78209152 210. 9753547 64. 34239489 20780 68. 39882433 441.7507389 191.5473306 567. 4880409 192. 6094197 1214 68. 38179055 128. 3025451 68.13347663 158. 5489338 45. 71421849 755 68. 37845059 34.87466691 29.79373274 64. 08006595 34. 39363901 16006 68. 36492377 71. 88449213 53.75743963 35. 40098018 17. 41759455 14138 68. 33603313 60.32285477 26. 70754215 75. 29445347 17. 84433561 15851 68. 32785024 317.1865116 273.6873358 160. 1095765 75. 57569123 21061 68. 32 67. 94 30. 57 46. 71 18. 28 23783 68. 29294768 395.5367742 88.22790322 467. 9801054 73. 38152003 15185 68. 29 234. 32 137. 00 142. 70 43. 80 8210 68. 29010872 744.1044707 212.872552 921. 2790683 180. 1467716 17104 68. 25904711 595.24177 185.1588591 458. 2361879 73. 95955511 17999 68. 24986223 901.7089805 380.2928546 1228. 53441 405. 2247232 18190 68. 24719026 182.2505082 61. 26301134 229. 5060244 48. 58869963 22602 68. 22998948 241.7042791 126.4784222 348. 9579426 102. 9813519 9082 68. 21328969 53.72565077 28. 46924103 38. 09238567 10. 55678356 16012 68. 18473305 93.81377915 55. 30071228 58. 55860103 14. 99778497 14989 68. 13580268 631.4437331 150.7953416 512. 7063086 97. 02311395 3987 68. 09589018 229.0363328 70.16578864 180. 4561841 37. 27169908 23837 68. 09 121. 06 52. 18 85. 23 27. 33 8317 68. 06 1149. 89 388. 88 1428. 19 346. 12 15302 68. 04929777 20.3076197 8.692629328 27. 81934381 10. 23548138 18001 67. 99802943 322.9223513 154.3838937 447. 9263548 164. 826114 16649 67. 97865767 147.8668375 84.05591013 97. 60434066 32. 64861331 22538 67. 96963979 268.3883299 96.52292148 356. 5133042 83. 51530908 24770 67. 9607889 167. 8615447 99. 9131833 258. 4592806 101. 0571212 23321 67. 95544497 543.4812122 158.9463892 669. 1827565 121. 2762102 5297 67. 89 282. 49 103. 56 368. 51 102. 45 1850 67. 86 62. 21 93. 09 24. 45 96. 13 17394 67. 81833971 452.0683779 169.8687842 324. 7418707 84. 03380507 13974 67. 81282878 486.1960174 343.7799181 277. 9765889 70. 48364801 16204 67. 80698385 1040. 091921 276.0342753 829. 9462579 117. 9912852 1754167. 781031. 81707. 66 671. 17 173. 64 12031 67. 78126618 168.7845658 59.30153211 130. 3205806 25. 6922294 23047 67. 77224829 56.55080604 20.02279821 70. 52393306 16. 27808767 20818 67. 76991032 1218.483928 808.490787 683. 4443517 312. 9826702 25718 67. 7640654 500.4365747 141.4001347 404. 9703762 60. 84572176 21657 67. 74970358 540.3602663 166.2162285 426. 2383025 80. 58986325 6055 67. 74953658 852.9112049 291.949659 1087. 752099 221. 2048224 825 67. 72899584 33.81589022 15.82849621 49. 46192808 17. 8340854 5838 67. 71229605 538.5143205 169.6443258 674. 9497738 122. 9308275 17175 67. 70394616 829.2548848 224.8030928 660. 0175001 115. 4189706 16726 67. 70377916 870.2897617 304.5065136 1099. 441777 185. 69785 1546 67. 7007732 196.1735398 73. 15499669 253. 3459783 55. 85865002 17744 67.69208931 46.14572439 26.53139174 64. 03176308 23. 43213839 1836167. 6610277 621.8671848 267. 2018135 448. 8817377 121. 6090859 4451 67. 64933785 238.855669 88.60178484 300. 3323635 63. 64516262 18396 67. 6296321 90. 02171091 44.79575334 61. 70407738 16. 44084885 2554 67. 62946511 57.15798904 20.53670721 42. 64349823 12. 30989757 15190 67. 61810925 3108.275869 1723.862361 1862. 426944 876.4994172 18606 67. 59239158 847.3774987 254.5206766 660. 8042777 115. 149482 1529567. 57171. 0770. 81126. 3831. 75 Table 5M GLGC Identifier LDA Score Tox Group Mean Tox Group SD Non-Tox Group Mean Non-Tox Group SD 770 67. 50905963 701. 6100581 282. 7824207 933. 1963529 236.566298 Table 5N GLGC Identifier PLS Score 25024-0.03408754 21011 0. 005158207 8317 0. 00286913 15861 0. 01758436 15862 0. 01155703 15028-0.04786289 15154 0. 01881327 15296 0. 00676223 16518 0. 02598835 17764-0. 02342505 20711-0. 01317801 23778 0. 002304377 20795 0. 00146821 20817 0. 0314257 20833-0.004259089 20919-0.0198629 20920-0.007400703 21012-0.003223273 22351-0.008960611 15848-0.01718595 15849-0.04416249 15850-0.01030871 23837-0. 0118801 4312 0. 003691487 20864 0. 007678122 10241 0. 01076413 11434 0. 06352768 20801-0.01583562 15126-0. 002417698 15297-0. 006103148 15124 0. 01198701 16080 0. 02010419 21013-0.001557214 13479-0. 03089779 13480 0. 003500852 6780-0. 003917337 18989 0. 000967733 1475 0. 01773045 1321-0. 03506051 11955 0. 02492273 1920 0. 01128843 15189-0. 005276864 17765-0.02927309 4010 0. 0263635 23225 0. 01153367 11956-0.009530467 11755-0. 03076732 20713 0. 02154138 25057 0. 01553224 17378-0. 008536189 14956 0. 00635737 14957-0. 008478985 16468 0. 01178596 5733 0. 01442401 Table 5N GLGC Identifier PLS Score 4748 0. 00604811 4749-0.001180088 17758-0.01322739 1301-0. 03655559 15125-0.005030922 17541 0. 01180132 6406 0. 008492458 1598 0. 03642105 17805-0. 01636465 1537-0.02368897 16768 0. 005025752 17158-0.006618596 1037-0.03482728 17377 0. 009030169 8664 0. 005364025 15569-0.01163379 15408-0.004117654 15409 0. 02009719 4615-0. 0216485 16148-0. 007715343 21078-0.002250057 23109 0. 005140497 25064-0.02576101 1466-0.0115101 15741 0. 001858723 13723-0.03098842 1183 0. 007847724 1174-0. 02682282 1814-0.02409571 23445 0. 01268358 25069-0. 01803054 25070-0. 001117053 1247 0. 002905345 17301 0. 02169327 14346 0. 01814763 15017-0.005796293 634 0. 02392324 17806-0.03059827 15174 0. 02558445 20887 0. 003184597 20818 0. 03540093 33 0. 000687164 23523 0. 04827108 1853 0. 000184702 23987-0.009158069 21651-0.01072442 635 0. 01430005 14347 0. 007348958 25098 0. 01413377 17157 0. 002967211 17337 0. 03499423 15703 0. 003194804 15662-0. 01996508 139730. 01031566 Table 5N GLGC Identifier PLS Score 18075 0. 001804553 18076 0. 01474427 4234-0. 03231172 23625 0. 008422249 15243-0.009537201 25165 0. 004905388 3454-0.01269925 23045-0. 01042821 17326-0.01356372 17327-0. 01550095 22603 0. 01994649 117-0.01073836 16649-0.003848922 985-0.004571139 4011 0. 02594932 16007-0.03245922 16155-0.03767058 25198-0.04053008 744 0. 01448024 5496-1.62254E-05 5497-0.004547023 25204 0. 01864999 17535 0. 01886001 16156-0.01055435 4723-0. 02257333 2367 0. 00281055 2368 0. 0198073 6554-0. 01628744 12422-0. 003597185 12423-0. 01363361 25247 0. 02928529 20404-0.003382577 18956-0.03746372 2554 0. 001275564 3254-0.02432042 4003-0.01871112 25257-0.006161937 15281-0.02035118 1214 0. 01756383 18727-0.01572102 18246 0. 001154571 18452-0. 01337099 18453-0.007857254 20493 0. 01936436 5492-0.01191286 18028-0.03629819 1354 0. 009908063 25290 0. 02397325 20494-0.000954101 18750-0.02634051 25315-0. 03588133 3987 0. 009837479 20149-0. 04258657 22412-0.004335643 Table 5N GLGC Identifier PLS Score 22413-0.00221225 109-0.005122522 22411 0. 01450058 455-0.01210526 25405 0. 01309029 20298-0.05332408 1622-0. 003529147 21882 0. 006960723 7872-0.01691339 24615-0.003635782 25460-0. 007971963 25467-0.002433017 25468 0. 009742874 25469-0.01432337 16449-0. 000927568 16450 0. 004114473 5837-0.005018729 25480 0. 006534462 2548i 0. 03633816 4012 0. 02058364 10886-0.02500923 5493-0.00559364 15127 0. 01913647 14003 0. 00302135 355 0. 001723895 356-0. 01191485 16248 0. 02829451 15832-0. 003373712 1471-0. 007821926 18647-0. 00834588 25518-0. 01890072 9224-0. 009229792 15135 0. 03026445 25525 0. 01468858 18990 0. 002379164 16211-0. 01861134 1943 0. 01443373 25545-0. 02041409 21583-0.000591347 25546-0.006230616 10260-0.002039004 25563-0. 009749564 14121-0. 01940992 3609 0. 0020902 18005-0.000341325 16268-0.05654464 22196 0. 01060633 12014 0. 006231096 16708 0. 01482556 16398 0. 006464105 25632 0. 03466999 4957 0. 008092677 25643-0. 03402377 23300 0. 03958223 Table 5N GLGC Identifier PLS Score 1546 0.01170207 22675-0.008282468 818-0.01053171 1550 0. 01494726 1551 0. 02599436 20715 0. 01030098 16947 0. 02858744 20884-0.02730658 24778-0.02842167 25675-0.0203886 20810-0.02795083 15653-0. 00909295 25676-0.04245567 19244 0. 01925244 1069 0. 02009015 3202 0. 01047109 25682-0.03644181 25686 0. 01175157 20872 0. 005200382 15201 0. 01743058 9620 0. 009678062 20427-0.007203343 25691-0.01287446 25699-0. 01975985 10860-0.01890404 10267-0.01660402 5667 0. 003279787 18611-0.01685318 17175 0. 008473313 25702 0. 006244145 10109 0. 005310704 25707 0. 03233485 15875 0. 002634939 25719-0.01698852 4441 0. 01366032 13646 0. 01512804 23708 0. 000573755 20844-0. 00279304 22219 0. 003093927 16272-0. 004407614 25770-0.01879616 20173-0.007049952 407 0. 004526638 8663 0. 01127171 19824 1. 61079E-05 1921 0. 006592317 24428 0. 01721819 24438-0.00262423 18619 0. 005152837 24496-0.03948592 24567-0. 01201788 291-0. 02495906 24770-0.008714317 24843-0. 03153809 Table 5N GLGC Identifier PLS Score 24874 0. 02920487 18686 0. 01941361 43-0. 01441405 133 0. 04627691 24590-0. 01762193 16675 0. 03559083 13682 0. 003206818 417-0. 0215943 18008 0. 003835681 466-0. 003738717 24639-0.01283457 556-0.004202022 714 0. 005186919 729-0. 003318912 770 0. 01406266 797 0. 01683459 912-0.01437363 1928-0.007305755 1929 0. 01778287 16610 0. 01123602 24648 0. 004198686 1104 0. 02800208 1602 0. 01814398 8426-0. 0182353 1203-0.0288901 617-0.008825291 11692 0. 02179052 19997 0. 002543063 10071-0.01549941 16676 0. 0117799 19952 0. 004150428 15379-0. 02876546 25907 0. 03277824 19002-0.01186146 19943 0. 000162394 20082 0. 02651264 18078 0. 000639759 20839-0. 000873427 4259 0. 01316487 15385 0. 01291856 4242 0. 01189998 16435-0.000204926 16849 0. 02508564 15022 0. 02776678 8888 0. 01160653 1867-0.00064856 24329-0.03123893 1729-0.03759896 9541-0. 03444796 21696 0. 009596217 20812 0. 0196699 13938-0. 01164793 15434-0.006764275 15097 0. 001716813 Table 5N GLGC Identifier PLS Score 23362-0.0179409 17473-0.01096604 15616 0. 001493839 18713 0. 01234178 815-0.02093439 15247 0. 01110444 21950 0. 000306391 21682-0.006126722 20802-0.01220903 23709 0. 02399753 16510 0. 03670125 4449-0.00546298 18077 0. 0171604 17160 0. 01415535 2109-0.005310179 15190-0. 01250142 16918-0.01725919 23660-0.01086482 8749-0.03118036 18687 0. 003382211 21975 0. 01300874 21842 0. 001369081 15191 0. 01105956 20717 0. 01063375 3431-0.006921202 17570 0. 007088764 15259-0.01822124 17563-0.02220618 11829 0. 005354438 16081 0. 0205121 1474-0. 03084054 17448 0. 02467472 9125-0.01139344 17196-0. 06969452 8212 0. 02652411 20702 0. 002678285 573-0. 02872789 409-0. 007299354 4574-0.02958615 754-0.0157468 15468 0. 000192713 12700-0. 01010274 14124-0. 01342113 20126 0. 0146427 4450-0. 04028917 4451-0. 04007754 171970. 02424782 17198 0. 033739 16726 0. 01229342 23698 0. 01072602 23699 0. 005510382 1540 0. 02953147 19255-0. 02175437 19256-0. 047948 Table 5N GLGC Identifier PLS Score 20405 0. 02330483 20885-0. 003796437 46 0. 01204979 6055-0. 01505172 14997-0.01111345 24563 0. 002454691 24564-0.01268496 24651-0. 0234343 240-0.01207596 10878-0.05290645 17105 0. 02110802 1514 0. 007158728 15112-0.007915743 24900 0. 000776591 9109 0. 02180698 1427-0. 01731983 16683-0.02202782 3549-0.002275369 23524 0. 02175325 19825 0. 001300221 18958-0.009980402 20803-0.01980488 16871-0.02941303 12606-0. 006382196 1970-0 00636348 23826-0.001208646 20925 0. 01287874 20780-0.009828659 16895-0.01042923 1424 0. 01814117 20481-2. 73489E-05 1542 0. 01467805 17226 0. 04658792 17227 0. 03661337 1479-0. 02727375 1558 0. 001784993 1559-0.00440292 20753 0. 000428273 20865-0. 02611805 1306 0. 01473606 19543 0. 01029956 15872 0. 006396827 24640 0. 02250593 20597-0. 0072339 439 0. 002488504 20518-0.008984546 12903 0. 007889638 21562 0. 002491812 10248 0. 03579842 23606-0.000202168 21122 0. 005247012 21123 0. 01623291 570 0. 0196455 16847 0. 01145459 Table 5N GLGC Identifier PLS Score 16204 0. 02414009 16205 0. 008361849 23854-0.01483347 24626-0. 0146705 1885-0.01965638 13940 0. 000886116 18108-0.005199345 646-0.05841963 20513 0. 02871836 20483 0. 002659336 11849 0. 01031365 1977 0. 000325571 20772 0. 01157497 16448-0.01863292 18107 0. 0166564 755-0.03462439 16681 0. 0152882 4198 0. 02822708 4199 0. 004798302 16147 0. 01038541 17554-0. 02472233 16354 0. 02817476 945 0. 00993543 989-0.01391793 16407-0. 000955995 7914 0. 000102491 1419-0.04516254 24885 0. 01988852 7064-0. 005395484 17149 0. 02755652 17150 0. 03952128 17393-0. 005221711 17394-0. 00579925 1508-0.0102906 17284-0. 007007458 17285 0. 0214901 18501 0. 02471658 18502-0.03477159 4589-0.000894857 18597 0. 005855973 4594-0.01689378 16444 0. 02065756 20809-0.02390898 15411 0. 01785927 4467 0. 01709855 18070 0. 01584395 7488-0.02057392 24643-0.001264686 1509 0. 00454317 13005-0.006822573 1894-0.00274857 4254-0.01411081 1762-0. 01280683 1763-0. 003490757 Table 5N GLGC Identifier PLS Score 7784 0. 002189607 23961-0.005958063 20868-0. 01507699 20869-0.009079757 20699 0. 00043838 20700-0.004172502 11153-0.02787509 16948-0.003215995 1678 0. 000367942 1976 0. 01736856 17502 0. 01984278 17661-0.008856236 15580-0.02737185 17411-0.004684325 4178 0. 00538893 15150-0.007069793 11852-0.000403569 4809-0.03041049 19067-0.007720506 20582-0.04267649 22374-0.01256255 22927-0. 03448938 4222-0.0165522 7090-0.02020823 15927 6 41932E-05 11865-0.006393904 19402-0.04323217 16139-0. 009440685 6451 0. 006511471 16419-0. 01146098 18084-0.01723762 15371-0. 01097884 15376-0.008551695 15887-0.0465706 15888-0.007077734 15401 0. 03108703 18902-0.003807752 15505 0. 02092673 6153 0. 005509851 4361-0.000569115 4386 0. 02562726 24235 0. 000464768 9952-0.009126578 9071-0. 000939401 474-0.01146703 9091-0.0287723 17420 0. 002994313 11959 0. 01476976 17693 0. 01033417 17289-0.003851629 17290 0. 01185756 205220. 000628409 20523 0. 003173917 17249-0. 02066336 Table 5N GLGC Identifier PLS Score 16023 0. 006094849 17779-0.000918023 1159 0. 01132209 17630 0. 009499276 13420 0. 005331431 14595 0. 02173968 16529-0. 0408304 4482 0. 03541986 4484 0. 02414248 18190 0. 02839109 17717 0. 01780007 9027 0. 01143368 13647 0. 001145029 820-0.02052028 12016 0. 004811067 21695 0. 005617932 4499 0. 00030477 8599 0. 01191982 12275 0. 004126427 12276 0. 006840609 18274 0. 000625962 18275-0.006242172 4512 0. 01254979 15876 0. 0076095 17500-0.02208598 23783-0.003488245 13542-0. 001915889 22539 0. 006842911 23322-0. 002697228 12848-0.01525511 3853 0. 02945047 3439-0.01804814 12020 0. 01677873 3870 0. 007775934 548 0. 01829203 17752 0. 01777645 18967-0.03837527 7505 0. 00383637 9084-0.02018928 10540 0. 02506434 3895-0.01868215 18396 0. 01085198 18291 0. 01498073 23063-0.002563515 18361 0. 01949046 14309 0. 002836866 21007-0.003881654 23203 0. 001480229 4412 0. 01905504 21035-0.01397706 18462-0. 0280539 22386 0. 01780035 Table 6 Time of Sacrifice (hour post first or Compound Vechicle Dose (mg/kg) only dose) Route nephrotoxins amphotericin Saline 0.25,5 3, 6, 24 iv, once CCl4 Corn oil 1000 1, 3, 6, 24 oral, once ciprofibrate .5% carboxymethylcellulose 15 24 oral, once cyclosporin A Olive oil 5, 50 6, 24, 168, 336 oral, daily dantrolene Corn oil 50, 2000 6, 24, 336 oral, daily ethylene glycol Saline 700, 7000 6, 24, 336 oral, daily melcoxicam 0.5% methylcellulose 0.5, 10 6, 24, 336 oral, daily olsalazine 0.5% carboxymethylcellulose 140, 1400 (drug base) 6, 24, 336 oral, daily pentamidine isethionate 5% dextrose 3, 30 6, 24, 168, 336 ip, daily phenacetin 0.25% methylcellulose 60, 600 6, 24, 336 oral, daily propyleneimine Saline 3.2, 32.3 6, 24, 48 ip, once semustine Sesame oil 4, 40 6, 24, 168 sc, once suramin Saline 45, 450 6, 24, 96 iv, once tacrolimus Saline 0.5, 5 6, 24, 72, 168 im, daily negative controls ceftazidime Saline 800 6, 24, 72, 168 iv, once 17-alpha-ethinylestradiol Propylene glycol 1,5 6, 24, 120 sc, daily gemfibrozil 0.5% methylcellulose 50, 500 6, 24, 168 oral, daily phenobarbital Saline 8, 40 6, 24, 48 ip, daily streptonycin Saline 2, 80 6, 24, 168 im, daily tamoxifen 1% methylcellulose 11.3, 45 6, 24, 168, 336 oral, daily temozolomide 0.4% methylcellulose 30, 300 6, 24, 168 oral, once transplatin 5% dextrose 1,5 6, 24, 168 iv, once